32883-50-4

Basic information

• Product Name: 1-(3,4,5-trimethoxyphenyl)propan-2-ol
• Synonyms: 1-(3,4,5-trimethoxyphenyl)propan-2-ol
• CAS NO: 32883-50-4
• Molecular Weight: 226.273
• Mol File: 32883-50-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(3,4,5-trimethoxyphenyl)propan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3,4,5-trimethoxyphenyl)propan-2-ol(32883-50-4)
• EPA Substance Registry System: 1-(3,4,5-trimethoxyphenyl)propan-2-ol(32883-50-4)

Safety Data

• Hazardous Substances Data: 32883-50-4(Hazardous Substances Data)

Upstream product

• 20675-95-0 (E)-2,6,-dimethoxy-4-(prop-1-en-1-yl)phenol 
• 91-10-1 1,3-dimethoxy-2-hydroxy-benzene 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 5438-54-0 1,3-dimethoxy-2-[(prop-2-en-1-yl)oxy]benzene 
• 6627-88-9 4-allyl-2,6-dimethoxyphenol 
• 487-12-7 isoelemicin 

Downstream Products

• 885680-06-8 2-iodo-3,4,5-trimethoxyphenyl propan-2-ol 

Relevant articles and documents

Concise access toward chiral hydroxy phenylpropanoids: formal synthesis of virolongin B; kigelin; kurasoin A; 4-hydroxysattabacin, and actinopolymorphol A

A simple, two step strategy consisting of Sharpless asymmetric dihydroxylation followed by regioselective breaking of [Formula presented] bond is utilized to target key chiral intermediates of natural products virolongin B, kigelin, kurasoin A, 4-hydroxy-sattabacin, and actinopolymorphol A. Derivatives of enantiopure hydroxy phenyl propanoids and α-hydroxy Weinreb amides are synthesized. The reductive cleavage of [Formula presented] bond in a regioselective manner is obtained using Pd/C in methanol.