1362169-08-1

Basic information

• Product Name: C₃₃H₃₀F₆N₄O₃
• Synonyms: C₃₃H₃₀F₆N₄O₃
• CAS NO: 1362169-08-1
• Molecular Weight: 644.617
• Mol File: 1362169-08-1.mol

Chemical Properties

• CAS DataBase Reference: C₃₃H₃₀F₆N₄O₃(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₃H₃₀F₆N₄O₃(1362169-08-1)
• EPA Substance Registry System: C₃₃H₃₀F₆N₄O₃(1362169-08-1)

Safety Data

• Hazardous Substances Data: 1362169-08-1(Hazardous Substances Data)

Upstream product

• 287979-82-2 (R)-(6-methoxyquinolin-4-yl)((1S,2R,4S,5R)-5-vinylquinuclidin-2-yl)methanamine 
• 1073917-05-1 3-((3,5-bis(trifluoromethyl)benzyl)amino)-4-methoxycyclobut-3-ene-1,2-dione 
• 287979-82-2 9-amino-9-deoxyepiquinidine 

Relevant articles and documents

Chiral squaramide catalyzed synthesis of C4 substituted chiral pyrazol-3-ol derivatives via a facile asymmetric Michael addition of 3-methyl-2-pyrazolin-5-one to β-nitrostyrenes

Asymmetric Michael addition of 3-methyl-2-pyrazolin-5-one to β-nitrostyrenes, catalyzed by a series of chiral squaramide bifunctional catalysts derived from cinchona alkaloids, yielded chiral pyrazol-3-ol derivatives. These pyrazol-3-ol derivatives were o

First example of quinine-squaramide catalyzed enantioselective addition of diphenyl phosphite to ketimines derived from isatins

A highly enantioselective addition of diphenyl phosphite to ketimines derived from isatins has been achieved using a bifunctional organocatalyst, quinine-derived squaramide catalyst. This method works efficiently with several ketimines to produce the corresponding 3-amino-2-oxoindolin-3-yl-phosphonates in excellent yields with high enantioselectivity (up to 98% ee). This journal is The Royal Society of Chemistry 2014.