61198-44-5

Basic information

• Product Name: Benzenepropanoic acid, b-ethyl-2-methoxy-, (R)-
• CAS NO: 61198-44-5
• Molecular Formula: C12H16O3
• Molecular Weight: 208.257
• Mol File: 61198-44-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, b-ethyl-2-methoxy-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, b-ethyl-2-methoxy-, (R)-(61198-44-5)
• EPA Substance Registry System: Benzenepropanoic acid, b-ethyl-2-methoxy-, (R)-(61198-44-5)

Safety Data

• Hazardous Substances Data: 61198-44-5(Hazardous Substances Data)

Upstream product

• 1226151-27-4 C₁₂H₁₈O₂ 
• 447461-90-7 (R)-3-(4-dimethylamino-2-methoxy-phenyl)-pentanal 
• 447461-91-8 (R)-3-(2-Methoxy-phenyl)-pentan-1-ol 
• 61198-40-1 (4S)-4r-methoxymethyl-2-(2-methoxy-trans-styryl)-5t-phenyl-4,5-dihydro-oxazole 
• 811-49-4 ethyllithium 
• 854647-56-6 2-(2-methoxy-phenyl)-butyric acid 
• 93-25-4 2-methoxyphenylacetic acid 
• 5561-92-2 1-(2-methoxyphenyl)propan-1-one 
• 99109-29-2 4-ethyl-2H-1-benzopyran-2-one 
• 135-02-4 ortho-anisaldehyde 
• 1576-87-0 trans-2-pentenal 
• 15799-79-8 3-methoxy-N,N-dimethylaniline 

Downstream Products

• 61198-58-1 (R)-(-)-3-(o-Anisyl)pentansaeuremethylester 

Relevant articles and documents

ANTI-HCMV COMPOSITIONS AND METHODS

This document relates to compounds useful as agents for preventing or treating human cytomegalovirus (HCMV) infections.

The enantioselective organocatalytic 1,4-addition of electron-rich benzenes to α,β-unsaturated aldehydes

The first enantioselective organocatalytic alkylation of electron-rich benzene rings with α,β-unsaturated aldehydes has been accomplished. The use of iminium catalysis has provided a new strategy for the enantioselective construction of benzylic stereogenicity, an important chiral synthon for natural product and medicinal agent synthesis. The (2S,5S)-5-benzyl-2-tert-butylimidazolidinone amine catalyst has been found to mediate the conjugate addition of a wide variety of substituted and unsubstituted anilines to unsaturated aldehydes. A diverse spectrum of aldehyde substrates can also be accommodated in this new organocatalytic transformation. While catalyst quantities of 10 mol % were generally employed in this study, successful alkylations conducted with catalyst loadings as low as 1 mol % are described. Copyright