Brief introduction of 6302-02-9

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,6302-02-9, its application will become more common.

Electric Literature of 6302-02-9, In the chemical reaction process,reaction time,type of solvent,can easily affect the result of the reaction, thereby determining the yield and properties of the reaction product.An updated downstream synthesis route of 6302-02-9 as follows.

EXAMPLE 19 2-Guanidino-4-methyl-5-(2-pyridyl)thiazole (0.16 g) was obtained according to substantially the same manner as that of Example 17 from 1-(2-pyridyl)acetone (2.8 g) and N-amidinothiourea (1.18 g). mp 166-168 C. IR (Nujol): 3440, 3400, 3270, 3080, 1630, 1600, 1580, 1540, 1520, 1420, 1320, 1240 cm-1 NMP (DMSO-d6, delta): 2.42 (3H, s), 6.8-7.1 (1H, m), 7.36 (1H, d, J=7 Hz), 7.5-7.8 (1H, m), 8.33 (1H, d d., J=2 Hz, 7 Hz) Mass. 233 (M+)

These compound has a wide range of applications. It is believed that with the continuous development of the source of the synthetic route,6302-02-9, its application will become more common.

Reference:
Patent; Fujisawa Pharmaceutical Co., Ltd.; US4649146; (1987); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Brief introduction of 6302-02-9

With the rapid development of chemical substances, we look forward to future research findings about 6302-02-9.

The major producers of chemicals have been the Europe, Japan and China. Due to the growing call for a cleaner, greener environment, people will have to find innovative ways to maintain their relevance. Here is a compound 6302-02-9, name is 1-(Pyridin-2-yl)propan-2-one. This compound has unique chemical properties. The synthetic route is as follows. Computed Properties of C8H9NO

EXAMPLE 15 2-Methylamino-4-methyl-5-(2-pyridyl)thiazole (1.8 g) was obtained according to substantially the same manner as that of Example 11 from 1-(2-pyridyl)acetone (2.03 g) and N-methylthiourea (2.7 g). mp 279-282 C. IR (Nujol): 3170, 1620, 1580, 1550, 1295, 1280 cm-1 NMR (D2 O+DCl, delta): 2.46 (3H, s), 3.20 (3H, s), 8.0-9.0 (4H, m) Mass. 205 (M+)

With the rapid development of chemical substances, we look forward to future research findings about 6302-02-9.

Reference:
Patent; Fujisawa Pharmaceutical Co., Ltd.; US4649146; (1987); A;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

New downstream synthetic route of 6302-02-9

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 6302-02-9, 1-(Pyridin-2-yl)propan-2-one.

6302-02-9, Each compound has different characteristics, and only by selecting the characteristics of the compound suitable for a specific situation can the compound be applied on a large scale. 6302-02-9, name is 1-(Pyridin-2-yl)propan-2-one. This compound has unique chemical properties. The synthetic route is as follows.

EXAMPLE 42 2-[(Aminocarbonyl)amino]-4-methyl-5-(2-pyridyl)-3-thiophenecarboxamide Prepared by the method of Example 26 from (2-pyridyl)acetone. MS (ES) 275 (M-H)-. 1H NMR (DMSO-D6) 9.9 (1H, s) 8.5 (1H, m), 7.8 (1H, m), 7.5 (1H, m), 7.4 (2H, m), 7.2 (2H, m), 6.7 (2H, m).

While traditionally a conservative industry, chemical producers will need to modernize their PR strategies to stay relevant.we look forward to future research findings about 6302-02-9, 1-(Pyridin-2-yl)propan-2-one.

Reference:
Patent; Baxter, Andrew; Brough, Stephen; Faull, Alan; Johnstone, Craig; McInally, Thomas; US2002/107252; (2002); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem