412909-31-0

Basic information

• Product Name: 5-(2,2-dimethoxy-ethyl)-2-methoxy-N-(4-trifluoromethyl-benzyl)-benzamide
• Synonyms: 5-(2,2-dimethoxy-ethyl)-2-methoxy-N-(4-trifluoromethyl-benzyl)-benzamide
• CAS NO: 412909-31-0
• Molecular Weight: 397.394
• Mol File: 412909-31-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-(2,2-dimethoxy-ethyl)-2-methoxy-N-(4-trifluoromethyl-benzyl)-benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2,2-dimethoxy-ethyl)-2-methoxy-N-(4-trifluoromethyl-benzyl)-benzamide(412909-31-0)
• EPA Substance Registry System: 5-(2,2-dimethoxy-ethyl)-2-methoxy-N-(4-trifluoromethyl-benzyl)-benzamide(412909-31-0)

Safety Data

• Hazardous Substances Data: 412909-31-0(Hazardous Substances Data)

Upstream product

• 3300-51-4 p-Trifluoromethylbenzylamine 
• 78515-16-9 methyl 5-formyl-2-methoxybenzoate 
• 412909-30-9 5-(2,2-dimethoxy-ethyl)-2-methoxy-benzoic acid methyl ester 

Downstream Products

• 433734-57-7 (E)-4-[4-Methoxy-3-(4-trifluoromethyl-benzylcarbamoyl)-phenyl]-but-2-enoic acid methyl ester 
• 433734-51-1 4-[4-methoxy-3-(4-trifluoromethyl-benzylcarbamoyl)-phenyl]-butyric acid methyl ester 

Relevant articles and documents

Design, synthesis and evaluation of substituted phenylpropanoic acid derivatives as peroxisome proliferator-activated receptor (PPAR) activators: Novel human PPARα-selective activators

A series of substituted phenylpropanoic acid derivatives was prepared as part of a search for subtype-selective human peroxisome proliferator-activated receptor (PPAR) activators. Structure-activity relationship studies indicated that the substituent at the α-position of the carboxyl group plays a key role in determining the potency and the selectivity for PPAR transactivation.