Day: September 21, 2022

Pyridine is diamagnetic and has a diamagnetic susceptibility of −48.7 × 10−6 cm3·mol−1.The molecular electric dipole moment is 2.2 debyes. 31181-90-5, formula is C6H4BrNO, Name is 5-Bromopicolinaldehyde. TThe standard enthalpy of formation is 100.2 kJ·mol−1 in the liquid phase and 140.4 kJ·mol−1 in the gas phase. Application of C6H4BrNO.

Han, Shi-Long;Yang, Jian;Tripathy, Debakanta;Guo, Xiao-Qing;Hu, Shao-Jun;Li, Xiao-Zhen;Cai, Li-Xuan;Zhou, Li-Peng;Sun, Qing-Fu research published 《 Self-Assembly of Lanthanide-Covalent Organic Polyhedra: Chameleonic Luminescence and Efficient Catalysis》, the research content is summarized as follows. A series of multinuclear lanthanide-covalent organic polyhedra (LnCOPs), including pillar-typed triangular prisms 1-Ln₃ and tetrahedra 2-Ln₄ (Ln = La^III, Sm^III, Eu^III), have been constructed for the first time, through either one-pot subcomponent self-assembly or post-assembly metalation. In contrast to the known tetrahedral cages based on transition metals, the pillar-typed polyhedra were favored from the same organic components in the presence of lanthanides. Besides this, facile transmetalations between the 1-Ln₃ polyhedra endow cascade chameleonic luminescence. Meanwhile, the open metal sites and pendent amine groups on 1-Ln₃ enable these polyhedra to catalyze the Henry reaction efficiently. A series of multinuclear lanthanide-covalent organic polyhedra (LnCOPs) have been synthesized, which demonstrate chameleonic luminescence by trans-metalation. Besides this, the open metal sites and pendent amine groups enable these LnCOPs to catalyze the Henry reaction efficiently.

31181-90-5, 5-Bromopyridine-2-carbaldehyde is a useful research compound. Its molecular formula is C6H4BrNO and its molecular weight is 186.01 g/mol. The purity is usually 95%.

5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%., Application of C6H4BrNO

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is colorless, but older or impure samples can appear yellow. 31181-90-5, formula is C6H4BrNO, Name is 5-Bromopicolinaldehyde. The pyridine ring occurs in many important compounds, including agrochemicals, pharmaceuticals, and vitamins. Historically, pyridine was produced from coal tar. Application In Synthesis of 31181-90-5.

Hall, David;Rajamalli, Pachaiyappan;Duda, Eimantas;Suresh, Subeesh Madayanad;Rodella, Francesco;Bagnich, Sergey;Carpenter-Warren, Cameron L.;Cordes, David B.;Slawin, Alexandra M. Z.;Strohriegl, Peter;Beljonne, David;Kohler, Anna;Olivier, Yoann;Zysman-Colman, Eli research published 《 Substitution Effects on a New Pyridylbenzimidazole Acceptor for Thermally Activated Delayed Fluorescence and Their Use in Organic Light-Emitting Diodes》, the research content is summarized as follows. In this work a new acceptor is used for use in thermally activated delayed fluorescence (TADF) emitters, pyridylbenzimidazole, which when coupled with phenoxazine allows efficient TADF to occur. N-functionalization of the benzimidazole using Me, Ph, and tert-Bu groups permits color tuning and suppression of aggregation-caused quenching (ACQ) with minimal impact on the TADF efficiency. The functionalized derivatives support a higher doping of 7 wt% before a fall-off in photoluminescence quantum yields is observed, in contrast with the parent compound, which undergoes ACQ at doping concentrations greater than 1 wt%. Complex conformational dynamics, reflected in the time-resolved decay profile, is found. The singlet-triplet energy gap, ΔE_ST, is modulated by N-substituents of the benzimidazole and ranges of between 0.22 and 0.32 eV in doped films. Vacuum-deposited organic light-emitting diodes, prepared using three of the four analogs, show maximum external quantum efficiencies, EQE_max, of 23.9%, 22.2%, and 18.6% for BIm(Me)PyPXZ, BIm(Ph)PyPXZ, and BImPyPXZ, resp., with a correlated and modest efficiency roll-off at 100 cd m^-2 of 19% 13%, and 24% of the EQE_max, resp.

31181-90-5, 5-Bromopyridine-2-carbaldehyde is a useful research compound. Its molecular formula is C6H4BrNO and its molecular weight is 186.01 g/mol. The purity is usually 95%.

5-Bromopyridine-2-carbaldehyde is a water soluble organic molecule that has been shown to inhibit the mitochondrial respiratory chain. It is a structural analog of the natural substrate for mitochondrial cytochrome c oxidase, 5-aminolevulinic acid. This compound has been shown to be selective against cancer cells and has anti-viral properties. The photophysical properties of 5-bromopyridine-2-carbaldehyde have been studied extensively. The fluorescence quantum yield of this molecule in aqueous solution is 0.06%., Application In Synthesis of 31181-90-5

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell. Quality Control of 1603-41-4.

Hagimori, Masayori;Yoshida, Tatsusada;Nishimura, Yasuhisa;Ogawa, Yukiko;Tanaka, Keitaro research published 《 Syntheses of novel pyridine-based low-molecular-weight luminogens possessing aggregation-induced emission enhancement (AIEE) properties》, the research content is summarized as follows. Novel pyridine-based fluorescing compounds, viz. pyrido[1,2-a]pyrrolo[3,4-d]pyrimidines I [R = H, Me] and N-methyl-4-((pyridin-2-yl)amino)maleimides II [R¹ = F, CN, Br, etc.] were selectively prepared by a one-pot reaction between a functionalized maleimide and 2-aminopyridines with electron-donating or electron-withdrawing groups at position 5 and were investigated photophys. and computationally. The photophys. studies revealed that all the synthesized compounds I and II exhibited fluorescence in organic solvents, while compounds II, which were based on an acceptor-donor-acceptor (A-D-A) system, exhibited aggregation-induced emission enhancement (AIEE) properties in aqueous media. Compounds II [R¹ = Br, CF₃] showed 7.0 and 15 times fluorescence enhancement. Time-dependent d. functional theory (TD-DFT) calculations were performed to gain better insight into the electronic nature of the compounds I [R = H] and II [R¹ = Br, CF₃] with and without AIEE properties.

Quality Control of 1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, 1603-41-4.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

At 25 °C pyridine has a viscosity of 0.88 mPa/s and thermal conductivity of 0.166 W·m−1·K−1. 16133-25-8, formula is C5H4ClNO2S, Name is Pyridine-3-sulfonyl chloride. The enthalpy of vaporization is 35.09 kJ·mol−1 at the boiling point and normal pressure.The enthalpy of fusion is 8.28 kJ·mol−1 at the melting point. Recommanded Product: Pyridine-3-sulfonyl chloride.

Guzelj, Samo;Gobec, Martina;Urbancic, Dunja;Mlinaric-Rascan, Irena;Corsini, Emanuela;Jakopin, Ziga research published 《 Structural features and functional activities of benzimidazoles as NOD2 antagonists》, the research content is summarized as follows. To gain insight into the structure-activity relationships of NOD2 antagonists, a series of novel analogs was designed and synthesized, and then screened for antagonist activity vs. NOD2, and counter-screened vs. NOD1. N-(2,3-Dihydro-1H-indene-5-yl)-2-(2-(2-(phenylsulfonamido)ethyl)-1H-benzo [d]imidazole-l-yl)acetamide and N-(2,3-dihydro-1H-indene-5-yl)-2-(2-(2-(phenylsulfonamido)ethyl)-1H-benzo [d]imidazole-l-yl)acetamide were identified as potent and moderately selective NOD2 antagonists, and N-(2,3-dihydro-1H-indene-5-yl)-2-(2-(2-((5-(dimethylamino)naphthalene)-1-sulfonamido)ethyl)-1H-benzo[d]imidazole-1-yl)acetamide and N-(2,3-dihydro-1H-inden-5-yl)-2-(2-(3-(Nmethylphenylsulfonamido)propyl)-1H-benzo[d]imidazol-1-yl)acetamide as dual NOD1/NOD2 antagonists, with balanced activities against both targets in the low micromolar range. These data enable in-depth exploration of their structure-activity relationships and provide deeper understanding of the structural features required for NOD2 antagonism.

Recommanded Product: Pyridine-3-sulfonyl chloride, Pyridine-3-sulfonyl chloride is a useful research compound. Its molecular formula is C5H4ClNO2S and its molecular weight is 177.61 g/mol. The purity is usually 95%.
Pyridine-3-sulfonyl chloride is a reagent used in the synthesis of pyrimidine derivatives with anti-proliferative activity against negative breast cancer cells.
Pyridine-3-sulfonyl chloride is a chemical compound that binds to the active site of cytochrome P450 enzymes. It can be used to study the effects of matrix effect on reaction solution. Pyridine-3-sulfonyl chloride has been shown to have an UV absorption spectrum with a maximum at 280 nm and a p450 activity that is proportional to the concentration of human serum. This compound has been shown to inhibit kinase domain in vitro assays, which may have clinical relevance in the treatment of obesity., 16133-25-8.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. 5315-25-3, formula is C6H6BrN, Name is 2-Bromo-6-methylpyridine. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell. Application In Synthesis of 5315-25-3.

Guo, Shi-Yu;Yang, Fan;Song, Ting-Ting;Guan, Yu-Qing;Min, Xiang-Ting;Ji, Ding-Wei;Hu, Yan-Cheng;Chen, Qing-An research published 《 Photo-induced catalytic halopyridylation of alkenes》, the research content is summarized as follows. Here an atom-economical cross-coupling of halopyridines such as 2-chloropyridine, 2-iodopyridine, 2-bromo-6-methylpyridine, etc. and unactivated alkenes such as hex-1-ene, cyclopentene, ethenylcyclohexane, etc. under photo-redox catalysis to afford a series of alkene halopyridylation products e.g., I was reported. This protocol with mild and redox neutral conditions contributes broad substrate scope. As a complement to conventional Heck-type reaction, this radical process avoids the involvement of β-H elimination and thus useful pyridyl and halide groups could be simultaneously and regioselectively incorporated onto alkenes. The success depends on TFA-promoted domino photocatalytic oxidative quenching activation and radical-polar crossover pathway. Plausible mechanism is proposed based on mechanistic investigations. Moreover, the reserved C-X bonds of these products are beneficial for performing further synthetic elaborations.

Application In Synthesis of 5315-25-3, 2-Bromo-6-methylpyridine (2BMPy) is a bromopyridine derivative. It is formed when 2-chloro-6-methylpyridine is heated with bromotrimethylsilane. Its synthesis from various methods have been reported.
2-Bromo-6-methylpyridine is a building block in the preparation of nitrogen containing heterocyclic compounds.
2-Bromo-6-methylpyridine is an organic compound that belongs to the group of pyridinium halides. It is soluble in common solvents such as water, ethanol, and acetone. 2BMPy has been shown to act as a glutamate receptor antagonist and has been used in the study of glutamate receptors, including their subtypes. This chemical has also been shown to have antioxidant properties and can be used in the prevention of atherosclerosis., 5315-25-3.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine has a conjugated system of six π electrons that are delocalized over the ring. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. The molecule is planar and, thus, follows the Hückel criteria for aromatic systems. SDS of cas: 1603-41-4.

Guo, Lina;Su, Meiyun;Lv, Junliang;Liu, Wenjie;Wang, Shaohua research published 《 N-Iodosuccinimide-promoted Regioselective Selenylation of 4H-Pyrido-[1,2-a]-pyrimidin-4-ones with Diselenides at Room Temperature》, the research content is summarized as follows. A novel and efficient approach for the regioselective selenylation of 4H-pyrido-[1,2-a]-pyrimidin-4-ones with diselenides at room temperature was developed. This procedure was catalyzed by N-iodosuccinimide under metal-free conditions with a broad range of substrate scopes and affords C3 selenylation products in good to excellent yields. Furthermore, the sulfenylation with di-Ph disulfides and 4-methylbenzenethiol in this transformation was successful.

1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, SDS of cas: 1603-41-4

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. 766-11-0, formula is C5H3BrFN, Name is 5-Bromo-2-fluoropyridine. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell. COA of Formula: C5H3BrFN.

Guo, Cui;Sun, Dong-Wei;Yang, Shuang;Mao, Shen-Jie;Xu, Xiao-Hua;Zhu, Shou-Fei;Zhou, Qi-Lin research published 《 Iridium-Catalyzed Asymmetric Hydrogenation of 2-Pyridyl Cyclic Imines: A Highly Enantioselective Approach to Nicotine Derivatives》, the research content is summarized as follows. A highly efficient asym. hydrogenation of cyclic imines containing a pyridyl moiety was established by using iridium catalysts with chiral spiro phosphine-oxazoline ligands. This process will facilitate the development of new nicotine-related pharmaceuticals I [R = 6-F, 6-Cl, 6-Me, etc; n = 1, 2, 3]. The introduction of a substituent at the ortho position of the pyridyl ring to reduce its coordinating ability ensures the success of the hydrogenation and excellent enantioselectivity.

COA of Formula: C5H3BrFN, 5-Bromo-2-fluoropyridine is a useful research compound. Its molecular formula is C5H3BrFN and its molecular weight is 175.99 g/mol. The purity is usually 95%.
5-Bromo-2-fluoropyridine is a boronic acid that has been shown to react with iodides and form 5-bromo-2-fluoroiodobenzene. The reaction of 5-bromo-2-fluoropyridine with benzene gives the same product as the reaction with 1,3,5-trioxane. The UV absorption of 5-bromo-2-fluoropyridine is found at 230 nm and 260 nm. It also has an absorption band in the infrared region at 1625 cm−1. Vibrational progressions have been observed for this molecule, which are due to dipole moments and electron density distributions in the molecule.
5-bromo-2-fluoropyridine is used in the synthesis of heteroaromatic and aniline derivatives of piperidines as potent ligands used for vesicular acetylcholine transport. , 766-11-0.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Pyridine is colorless, but older or impure samples can appear yellow. 5315-25-3, formula is C6H6BrN, Name is 2-Bromo-6-methylpyridine. The pyridine ring occurs in many important compounds, including agrochemicals, pharmaceuticals, and vitamins. Historically, pyridine was produced from coal tar. Synthetic Route of 5315-25-3.

Gujral, Gurjeet;Bhasin, Aman K. K.;Bhasin, K. K.;Gulati, Shivani research published 《 Syntheses, characterization, and single crystal X-ray analysis of 2-pyridyl aryl selenium (IV) bromides and chlorides》, the research content is summarized as follows. A variety of sym. and unsym. 2-pyridyl aryl selenium (IV) chlorides or bromides were prepared by the dropwise addition of a dilute solution of bromine or sulfuryl chloride to the corresponding 2-pyridyl aryl selenide in dried organic solvent with continuous stirring at 0°. Removal of the solvent under reduced pressure gave, 2-pyridyl aryl selenium (IV) bromides or chlorides, resp., in quant. yields. The titled dihalides prepared were characterized by elemental anal., spectroscopic studies, and single crystal x-ray anal. Single crystal x-ray anal. revealed that the 2-pyridyl aryl selenium (IV) bromides/chlorides have a distorted trigonal bipyramidal structure. The pyridyl and Ph rings along with a lone pair of electrons on selenium are at equatorial positions whereas chloride/bromide atoms at axial positions of the distorted trigonal bipyramidal structure.

5315-25-3, 2-Bromo-6-methylpyridine (2BMPy) is a bromopyridine derivative. It is formed when 2-chloro-6-methylpyridine is heated with bromotrimethylsilane. Its synthesis from various methods have been reported.
2-Bromo-6-methylpyridine is a building block in the preparation of nitrogen containing heterocyclic compounds.
2-Bromo-6-methylpyridine is an organic compound that belongs to the group of pyridinium halides. It is soluble in common solvents such as water, ethanol, and acetone. 2BMPy has been shown to act as a glutamate receptor antagonist and has been used in the study of glutamate receptors, including their subtypes. This chemical has also been shown to have antioxidant properties and can be used in the prevention of atherosclerosis., Synthetic Route of 5315-25-3

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

The critical parameters of pyridine are pressure 6.70 MPa, temperature 620 K and volume 229 cm3·mol−1. 5315-25-3, formula is C6H6BrN, Name is 2-Bromo-6-methylpyridine. In the temperature range 340–426 °C its vapor pressure p can be described with the Antoine equation.. Recommanded Product: 2-Bromo-6-methylpyridine.

Gujral, Gurjeet;Bhasin, K. K.;Gulati, Shivani research published 《 A new synthetic methodology for the preparation 2-Pyridyl anisyl/benzyl selenides: X-Ray Crystal Structure of 2-(4-Methyl pyridyl)tolyl selenide》, the research content is summarized as follows. An effective methodol. for the synthesis of these selenides had been developed by reacting dianisyl/dibenzyl diselenide with substituted/unsubstituted 2-pyridyl halides in the presence of activated magnesium metal, Cu₂O, and bipyridyl in DMF at 110°C for 18-20 h. The newly synthesized 2-pyridyl anisyl/benzyl selenides were either viscous liquids or crystalline solids that were stable at room temperature for several months without decomposition These were fully characterized by various spectroscopic techniques, namely, NMR (¹H, ¹³C, and ⁷⁷Se), IR, and mass spectroscopy. Single-crystal X-ray diffraction study of 2-(4-methylpyridyl) tolyl selenide was carried out to know the structural details of the mol. and well-defined diffraction quality crystals of 2-(4-Me pyridyl)tolyl selenide were obtained by slow evaporation of saturated solution of the compound in hexane-dichloromethane solvent mixture (4:1, volume/volume).

Recommanded Product: 2-Bromo-6-methylpyridine, 2-Bromo-6-methylpyridine (2BMPy) is a bromopyridine derivative. It is formed when 2-chloro-6-methylpyridine is heated with bromotrimethylsilane. Its synthesis from various methods have been reported.
2-Bromo-6-methylpyridine is a building block in the preparation of nitrogen containing heterocyclic compounds.
2-Bromo-6-methylpyridine is an organic compound that belongs to the group of pyridinium halides. It is soluble in common solvents such as water, ethanol, and acetone. 2BMPy has been shown to act as a glutamate receptor antagonist and has been used in the study of glutamate receptors, including their subtypes. This chemical has also been shown to have antioxidant properties and can be used in the prevention of atherosclerosis., 5315-25-3.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

The critical parameters of pyridine are pressure 6.70 MPa, temperature 620 K and volume 229 cm3·mol−1. 1603-41-4, formula is C6H8N2, Name is 2-Amino-5-methylpyridine. In the temperature range 340–426 °C its vapor pressure p can be described with the Antoine equation.. Application In Synthesis of 1603-41-4.

Gui, Qing-Wen;Wang, Bin-Bin;Zhu, Sha;Li, Fu-Long;Zhu, Meng-Xue;Yi, Min;Yu, Jia-Ling;Wu, Zhi-Lin;He, Wei-Min research published 《 Four-component synthesis of 3-aminomethylated imidazoheterocycles in EtOH under catalyst-free, oxidant-free and mild conditions》, the research content is summarized as follows. With green ethanol as the sole solvent, 3-aminomethylated imidazoheterocycles I [R¹ = H, 6-Me, 7-Me, etc.; R² = Ph, 4-ClC₆H₄, 2-furanyl, etc.; R³ = Bn, n-Bu, CH₂CH₂CN, etc.; R⁴ = H, Me, i-Pr, etc.; R³R⁴ = CH₂(CH₂)₂CH₂, CH₂(CH₂)CH₂, CH₂CH₂OCH₂CH₂, R³ = R⁴ = Et, i-Pr] were synthesized via a four-component reaction of 2-aminopyridines with 2-bromoacetophenones dichloromethane and amines at ambient temperature under metal-free, oxidant-free and mild conditions.

Application In Synthesis of 1603-41-4, 2-Amino-5-methylpyridine, also known as 2-Amino-5-methylpyridine, is a useful research compound. Its molecular formula is C6H8N2 and its molecular weight is 108.14 g/mol. The purity is usually 95%.
2-Amino-5-methylpyridine is a chemical compound that belongs to the group of methyl ketones. It has a nitrogen atom and an oxygen atom in its structure, which allows it to form hydrogen bonds with other molecules. 2-Amino-5-methylpyridine can be obtained by reacting hydrochloric acid and xanthone in the presence of a base. The compound is highly reactive and has been shown to have antiinflammatory properties. This can be attributed to its ability to inhibit prostaglandin synthesis. 2-Amino-5-methylpyridine also has fluorescence properties that are sensitive to pH changes and can be used as a probe for metal ions. 2-Amino-5-methylpyridine is an organic compound that contains a methyl group, two nitrogen atoms, and one oxygen atom in its chemical structure. This molecule can form hydrogen bonds with other molecules due to its nitrogen atoms and oxygen atom,, 1603-41-4.

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem