1191954-40-1

Basic information

• Product Name: (S,S)-2-sec-butyl-3-methoxy-6-(trifluoromethyl)pyridin-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
• Synonyms: (S,S)-2-sec-butyl-3-methoxy-6-(trifluoromethyl)pyridin-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate
• CAS NO: 1191954-40-1
• Molecular Weight: 465.392
• Mol File: 1191954-40-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S,S)-2-sec-butyl-3-methoxy-6-(trifluoromethyl)pyridin-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S,S)-2-sec-butyl-3-methoxy-6-(trifluoromethyl)pyridin-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate(1191954-40-1)
• EPA Substance Registry System: (S,S)-2-sec-butyl-3-methoxy-6-(trifluoromethyl)pyridin-4-yl 3,3,3-trifluoro-2-methoxy-2-phenylpropanoate(1191954-40-1)

Safety Data

• Hazardous Substances Data: 1191954-40-1(Hazardous Substances Data)

Upstream product

• 25570-03-0 (+)-(S)-2-methylbutane nitrile 
• 1191954-35-4 (S)-2-sec-butyl-3-methoxy-6-(trifluoromethyl)pyridin-4(1H)-one 
• 20445-33-4 (R)-methoxytrifluoromethylphenylacetyl chloride 

Relevant articles and documents

A practical two-step procedure for the preparation of enantiopure pyridines: Multicomponent reactions of alkoxyallenes, nitriles and carboxylic acids followed by a cyclocondensation reaction

A practical approach to highly functionalized 4-hydroxypyridine derivatives with stereogenic side chains in the 2- and 6-positions is described. The presented two-step process utilizes a multicomponent reaction of alkoxyallenes, nitriles and carboxylic ac