107291-10-1

Basic information

• Product Name: (+)-(2S,3S)-4-(benzyloxy)-2,3-dimethoxy-1-butanol
• Synonyms: (+)-(2S,3S)-4-(benzyloxy)-2,3-dimethoxy-1-butanol
• CAS NO: 107291-10-1
• Molecular Weight: 240.299
• Mol File: 107291-10-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (+)-(2S,3S)-4-(benzyloxy)-2,3-dimethoxy-1-butanol(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(2S,3S)-4-(benzyloxy)-2,3-dimethoxy-1-butanol(107291-10-1)
• EPA Substance Registry System: (+)-(2S,3S)-4-(benzyloxy)-2,3-dimethoxy-1-butanol(107291-10-1)

Safety Data

• Hazardous Substances Data: 107291-10-1(Hazardous Substances Data)

Upstream product

• 27957-93-3 (+)-(2R,3R)-diethyl di-O-methyltartrate 
• 24679-72-9 (2S,3S)-2,3-dimethoxy-1,4-butanediol 
• 100-39-0 benzyl bromide 

Downstream Products

• 115952-07-3 (3R,4R)-3,4-dimethoxy-1-phenylphospholane 
• 880359-09-1 1-O-benzyl-4-deoxy-4-ethoxy(phenyl)phosphinoyl-2,3-di-O-methyl-L-threitol 
• 880359-10-4 4-deoxy-4-ethoxy(phenyl)phosphinoyl-2,3-di-O-methyl-L-threitol 
• 880359-11-5 1-bromo-1,4-dideoxy-4-ethoxy(phenyl)phosphinoyl-2,3-di-O-methyl-L-threitol 
• 880359-08-0 1-O-benzyl-4-bromo-4-deoxy-2,3-di-O-methyl-L-threitol 
• 107291-11-2 (+)-(2S,3S)-1-(benzyloxy)-4-<(tert-butyldimethylsilyl)oxy>-2,3-dimethoxybutane 

Relevant articles and documents

A Synthetic Approach to (-)-Quassimarin Based on Intramolecular Diels-Alder Strategy

A novel approach to the tetracyclic precursor 32 for the total synthesis of (-)-quassimarin based on an intramolecular Diels-Alder strategy is described.The key tricyclic species 22 was constructed from the triene 6 via a highly endo-selective intramolecu

Synthetic studies toward antitumor quassinoids. 2.1 A chiral approach to quassimarin via intramolecular Diels-Alder reaction

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