482656-48-4

Basic information

• Product Name: ethyl (S)-3-(4-benzyloxyphenyl)-2-(4-tert-butylphenoxy)propionate
• Synonyms: ethyl (S)-3-(4-benzyloxyphenyl)-2-(4-tert-butylphenoxy)propionate
• CAS NO: 482656-48-4
• Molecular Weight: 432.56
• Mol File: 482656-48-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: ethyl (S)-3-(4-benzyloxyphenyl)-2-(4-tert-butylphenoxy)propionate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (S)-3-(4-benzyloxyphenyl)-2-(4-tert-butylphenoxy)propionate(482656-48-4)
• EPA Substance Registry System: ethyl (S)-3-(4-benzyloxyphenyl)-2-(4-tert-butylphenoxy)propionate(482656-48-4)

Safety Data

• Hazardous Substances Data: 482656-48-4(Hazardous Substances Data)

Upstream product

• 62517-34-4 ethyl 2-hydroxy-3-(4-hydroxyphenyl)propionate 
• 410079-50-4 (R)-3-(4-benzyloxyphenyl)-2-hydroxypropionitrile 
• 410079-54-8 ethyl (R)-3-(4-hydroxyphenyl)lactate 
• 40167-10-0 2-[4-(benzyloxy)phenyl]acetaldehyde 
• 223127-72-8 ethyl 3-(4-benzyloxyphenyl)-2-(4-tert-butylphenoxy)propionate 
• 141109-83-3 ethyl 3-(4-benzyloxyphenyl)lactate 
• 100-44-7 benzyl chloride 
• 98-54-4 para-tert-butylphenol 
• 482656-47-3 ethyl (2R)-3-[4-(benzyloxy)phenyl]-2-hydroxypropanoate 

Downstream Products

• 710327-30-3 ethyl (S)-2-(4-tert-butylphenoxy)-3-[4-[2-[(4-(pyridin-2-yl)benzoyl)amino]ethoxy]phenyl]propionate 
• 710327-29-0 ethyl (S)-3-[4-(2-tert-butoxycarbonylaminoethoxy)phenyl]-2-(4-tert-butylphenoxy)propionate 
• 482656-49-5 ethyl (S)-2-(4-tert-butylphenoxy)-3-(4-hydroxyphenyl)propionate 

Relevant articles and documents

NOVEL ANTIDIABETIC COMPOUNDS

The present invention provides novel compounds of the general formula (I), wherein the symbols are same as described in specification, their pharmaceutically acceptable salts, their tautomeric forms, their stereoisomers, pharmaceutical compositions containing them, to process and intermediates for the preparation of the above said compounds, having the utility of these compounds in medicine and to methods for their therapeutic use, and their use in the treatment of diabetes and related diseases.

Efficient synthesis of antihyperglycemic (S)-alpha-aryloxy-beta-phenylpropionic acid using a bifunctional asymmetric catalyst.

Antihyperglycemic (S)-alpha-aryloxy-beta-phenylpropionic acid was prepared using catalytic asymmetric cyanosilylation as a key reaction to construct alpha-oxycarboxylic acid moiety.