ChemicalBook >> CAS DataBase List >>5-Bromo-4-methyl-2-(trifluoromethyl)pyridine

5-Bromo-4-methyl-2-(trifluoromethyl)pyridine

CAS No.
1010422-51-1
Chemical Name:
5-Bromo-4-methyl-2-(trifluoromethyl)pyridine
Synonyms
3-bromo-4-methyl-6-(trifluoromethyl)pyridine;5-Bromo-4-methyl-2-(trifluoromethyl)pyridine;Pyridine, 5-bromo-4-methyl-2-(trifluoromethyl)-
CBNumber:
CB82534826
Molecular Formula:
C7H5BrF3N
Molecular Weight:
240.02
MDL Number:
MFCD18257679
MOL File:
1010422-51-1.mol
Last updated:2025-08-08 17:45:00
Product description Number Pack Size Price
5-Bromo-4-methyl-2-(trifluoromethyl)pyridine B679500 10mg $45
5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 95% PC900609 100mg $114
5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 95% 3H32-B-6K 100mg $125
5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 95% PC900609 250mg $182
5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 0321AA 100mg $197

5-Bromo-4-methyl-2-(trifluoromethyl)pyridine Properties

Boiling point 203℃
Density 1.614
Flash point 76℃
storage temp. Sealed in dry,Room Temperature
pka -1.17±0.30(Predicted)
Appearance Colorless to light yellow Liquid

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H319-H315-H335
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501
HS Code  2933399990

5-Bromo-4-methyl-2-(trifluoromethyl)pyridine price More Price(15)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B679500 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 1010422-51-1 10mg $45 2021-12-16 Buy
Apolloscientific PC900609 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 95% 1010422-51-1 100mg $114 2021-12-16 Buy
SynQuest Laboratories 3H32-B-6K 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 95% 1010422-51-1 100mg $125 2021-12-16 Buy
Apolloscientific PC900609 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 95% 1010422-51-1 250mg $182 2021-12-16 Buy
AK Scientific 0321AA 5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 1010422-51-1 100mg $197 2021-12-16 Buy
Product number Packaging Price Buy
B679500 10mg $45 Buy
PC900609 100mg $114 Buy
3H32-B-6K 100mg $125 Buy
PC900609 250mg $182 Buy
0321AA 100mg $197 Buy

5-Bromo-4-methyl-2-(trifluoromethyl)pyridine Chemical Properties,Uses,Production

Synthesis

2-Trifluoromethyl-5-bromopyridine

436799-32-5

Iodomethane

74-88-4

5-Bromo-4-methyl-2-(trifluoromethyl)pyridine

1010422-51-1

In a dry 250 mL three-necked round-bottomed flask equipped with a stir bar, thermometer and flushed with nitrogen, anhydrous THF (16 mL, Aldrich, no inhibitor) was added followed by N,N-diisopropylamine (0.895 g, 8.85 mmol, Aldrich, redistilled 99.95% pure). After cooling the stirred solution to -70 °C, n-butyllithium (3.54 mL of a 2.5 M hexane solution, 8.85 mmol) was added slowly and dropwise, keeping the reaction temperature below -60 °C. The resulting solution was continued to be stirred at -70 °C for 10 min, followed by warming to -20 °C and then rapidly cooled to -90 °C. A solution of 5-bromo-2-(trifluoromethyl)pyridine (2 g, 8.85 mmol) in anhydrous THF (8 mL, Aldrich, no inhibitor) was slowly added dropwise to ensure that the reaction temperature was below -85°C. The resulting orange solution was stirred at -90 °C for 40 min. In another dry 250 mL three-necked round-bottomed flask equipped with a stir bar, thermometer and flushed with nitrogen, anhydrous THF (5 mL, Aldrich, no inhibitor) was added, followed by iodomethane (5 mL, 80 mmol). After cooling the solution to -90 °C, the preformed lithiated pyridine solution was slowly added through a cannula, controlling the addition rate to keep the reaction temperature in the receiving flask below -80 °C. The resulting dark-colored solution was continued to be stirred at -90 °C for 15 min (LCMS showed completion of the reaction). The reaction mixture was quenched with saturated aqueous NaHCO3 followed by slow addition of NH4Cl solution (50 mL) and warmed to room temperature. The organic phase was extracted with EtOAc (2 x 50 mL) and the combined organic layers were washed sequentially with water (50 mL) and brine (50 mL), separated, dried with MgSO4 and filtered. Vacuum concentration afforded 1.68 g of brown oil, which was purified by short-range vacuum distillation (45-46 °C, ca. 5 mmHg) to give 5-bromo-4-methyl-2-(trifluoromethyl)pyridine (0.289 g, 14% yield) as a yellow oil (purity >97%). mS (M+H)+: 241.8, tR = 2.458 min (Method 1); 1H NMR (CDCl3) δ 8.74 (1H, s), 7.56 (1H, s), 2.50 (3H, s).

References

[1] Patent: WO2008/124610, 2008, A1. Location in patent: Page/Page column 45; 46
[2] Patent: WO2008/124614, 2008, A1. Location in patent: Page/Page column 37-38

5-Bromo-4-methyl-2-(trifluoromethyl)pyridine Preparation Products And Raw materials

5-Bromo-4-methyl-2-(trifluoromethyl)pyridine Suppliers

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5-Bromo-4-methyl-2-(trifluoromethyl)pyridine 3-bromo-4-methyl-6-(trifluoromethyl)pyridine Pyridine, 5-bromo-4-methyl-2-(trifluoromethyl)- 1010422-51-1