1280727-95-8

Basic information

• Product Name: isopropyl (E)-3,4-bis(benzyloxy) cinnamate
• Synonyms: isopropyl (E)-3,4-bis(benzyloxy) cinnamate
• CAS NO: 1280727-95-8
• Molecular Weight: 402.49
• Mol File: 1280727-95-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: isopropyl (E)-3,4-bis(benzyloxy) cinnamate(CAS DataBase Reference)
• NIST Chemistry Reference: isopropyl (E)-3,4-bis(benzyloxy) cinnamate(1280727-95-8)
• EPA Substance Registry System: isopropyl (E)-3,4-bis(benzyloxy) cinnamate(1280727-95-8)

Safety Data

• Hazardous Substances Data: 1280727-95-8(Hazardous Substances Data)

Upstream product

• 139-85-5 3,4-dihydroxybenzaldehyde 
• 100-44-7 benzyl chloride 
• 54429-62-8 (E)-3-(3,4-bis(benzyloxy)phenyl)acrylic acid 
• 67-63-0 isopropyl alcohol 
• 5447-02-9 3,4-dibenzyloxybenzaldehyde 

Downstream Products

• 1280727-96-9 isopropyl (2R,3S)-3-(3,4-bis(benzyloxy)phenyl)-2,3-dihydroxy propanoate 
• 1280727-97-0 isopropyl (2S,3R)-3-(3,4-bis(benzyloxy)phenyl)-2,3-dihydroxy propanoate 
• 950665-05-1 isopropyl (R)-3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate 
• 1280727-98-1 isopropyl (S)-3-(3,4-dihydroxyphenyl)-2-hydroxypropanoate 

Relevant articles and documents

Efficient and practical asymmetric synthesis of isopropyl (R)-3-(3′,4′-dihydroxyphenyl)-2-hydroxypropanoate and its enantiomer

The highly enantioselective synthesis of (R)-isopropyl 3-(3′, 4′-dihydroxyphenyl)-2-hydroxypropanoate and its enantiomer has been achieved starting from 3,4-dihydroxybenzaldehyde. The stereogenic centers were established through asymmetric dihydroxylation of (E)-isopropyl 3,4-bis(benzyloxy) cinnamate. A convenient manipulation in selective catalytic hydrogenation and deprotection was also accomplished in HCl-iPrOH employing 10% Pd/C catalyst.