657393-37-8

Basic information

• Product Name: 1,2-Propanediol, 1-(3,4,5-trimethoxyphenyl)-, (1S,2S)-
• CAS NO: 657393-37-8
• Molecular Formula: C12H18O5
• Molecular Weight: 242.272
• Mol File: 657393-37-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,2-Propanediol, 1-(3,4,5-trimethoxyphenyl)-, (1S,2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Propanediol, 1-(3,4,5-trimethoxyphenyl)-, (1S,2S)-(657393-37-8)
• EPA Substance Registry System: 1,2-Propanediol, 1-(3,4,5-trimethoxyphenyl)-, (1S,2S)-(657393-37-8)

Safety Data

• Hazardous Substances Data: 657393-37-8(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 835922-48-0 (S)-1-(3,4,5-trimethoxyphenyl)-2-propanol 
• 657393-30-1 (+)-(8R)-(2,6-dimethoxy-4-propenylphenoxy)-1-(3,4,5-trimethoxyphenyl)propan-1-one 
• 658706-47-9 (1R,2R)-2-[2,6-dimethoxy-4-((E)-prop-1-enyl)phenoxy]-1-(3,4,5-trimethoxyphenyl)propan-1-ol 
• 1027821-84-6 4-[(1R,2R)-2-Hydroxy-1-methyl-2-(3,4,5-trimethoxy-phenyl)-ethoxy]-3,5-dimethoxy-benzaldehyde 
• 657393-39-0 toluene-4-sulfonic acid (1S)-methyl-2-oxo-2-(3,4,5-trimethoxy-phenyl)-ethyl ester 
• 658706-64-0 (8R)-oxo-surinamensin 
• 91497-93-7 1-<3,4,5-Trimethoxy-phenyl>-propandion-(1,2) 
• 657393-38-9 (2S)-hydroxy-1-(3,4,5-trimethoxy-phenyl)-propan-1-one 

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.