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2-Methoxy-3-(trifluoromethyl)pyridine

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CAS:121643-44-5
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CAS:121643-44-5
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2-Methoxy-3-(trifluoromethyl)pyridine manufacturers

2-Methoxy-3-(trifluoromethyl)pyridine Basic information
storage Uses
Product Name:2-Methoxy-3-(trifluoromethyl)pyridine
Synonyms:2-Methoxy-3-(trifluoromethyl)pyridine 98%;2-Methoxy-3-(trifluoromethyl)pyridine98%;BUTTPARK 45\01-90;METHOXY-3-TRIFLUOROMETHYLPYRIDINE;3-(trifluoroMethyl)-2-Methoxypyridine;2-METHOXY-3-(TRIFLUOROMETHYL)PYRIDINE;2-Methoxy-3-(trifluoromethyl)pyridine>;2-Bromo-7-(trifluoromethyl)pyridine
CAS:121643-44-5
MF:C7H6F3NO
MW:177.12
EINECS:
Product Categories:C7 and C8;Heterocyclic Building Blocks;Pyridines;Pyridine
Mol File:121643-44-5.mol
2-Methoxy-3-(trifluoromethyl)pyridine Structure
2-Methoxy-3-(trifluoromethyl)pyridine Chemical Properties
Boiling point 44 °C
density 1.297 g/mL at 25 °C
refractive index n20/D 1.441
Fp 118 °F
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Methanol
form clear liquid
pka0.97±0.10(Predicted)
color Colorless to Almost colorless
InChIInChI=1S/C7H6F3NO/c1-12-6-5(7(8,9)10)3-2-4-11-6/h2-4H,1H3
InChIKeySSAZZVQVJJXPMB-UHFFFAOYSA-N
SMILESC1(OC)=NC=CC=C1C(F)(F)F
CAS DataBase Reference121643-44-5(CAS DataBase Reference)
Safety Information
Hazard Codes T,Xi,Xn
Risk Statements 10-25-36/37/38-20/21/22
Safety Statements 16-26-45-36
RIDADR UN 1992 3/PG 3
WGK Germany 3
HazardClass IRRITANT
PackingGroup III
HS Code 2933399990
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2-Methoxy-3-(trifluoromethyl)pyridine Usage And Synthesis
storage2-Methoxy-3-(trifluoromethyl)pyridine store at room temperature.
Uses2-Methoxy-3-(trifluoromethyl)pyridine belongs to pyridine derivatives and can be used as pharmaceutical intermediates.
Synthesis
Sodium Methoxide

124-41-4

2-Chloro-3-(trifluoromethyl)pyridine

65753-47-1

2-Methoxy-3-(trifluoromethyl)pyridine

121643-44-5

2-Chloro-3-trifluoromethylpyridine (3 g, 16.53 mmol) was dissolved in 30 mL of a methanol solution of sodium methanolate (5.4 M). The reaction mixture was stirred at room temperature for 48 hours. After completion of the reaction, the mixture was cooled in an ice bath and extracted three times with dichloromethane (DCM). The organic phases were combined, washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The organic phase was concentrated under reduced pressure to afford 2-methoxy-3-trifluoromethylpyridine as a colorless liquid (2.7 g, 89% yield). The product was characterized by 1H-NMR (400 MHz, DMSO-d6, 298 K): δ 3.98 (s, 3H), 7.2 (dd, 1H), 8.11 (d, 1H), 8.45 (d, 1H). Mass Spectrometry (MS): m/z 178.1 [M+1]+, retention time (Rt) = 1.29 min.

References[1] Patent: WO2013/57711, 2013, A1. Location in patent: Page/Page column 45-46
[2] Patent: WO2013/88404, 2013, A1. Location in patent: Page/Page column 92
[3] Patent: US2015/342951, 2015, A1. Location in patent: Paragraph 0841-0842
2-Methoxy-3-(trifluoromethyl)pyridine Preparation Products And Raw materials
Raw materialsSodium Methoxide-->2-Chloro-3-(trifluoromethyl)pyridine
Preparation ProductsLeniolisib-->5-bromo-2-methoxy-3-(trifluoromethyl)pyridine
Tag:2-Methoxy-3-(trifluoromethyl)pyridine(121643-44-5) Related Product Information
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