762261-99-4

Basic information

• Product Name: (3S,4R,5S)-5-(benzyloxy)-4-hydroxy-2-((trimethylsilyl)methyl)hex-1-en-3-yl diisopropylcarbamate
• CAS NO: 762261-99-4
• Molecular Weight: 435.679
• Mol File: 762261-99-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,4R,5S)-5-(benzyloxy)-4-hydroxy-2-((trimethylsilyl)methyl)hex-1-en-3-yl diisopropylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4R,5S)-5-(benzyloxy)-4-hydroxy-2-((trimethylsilyl)methyl)hex-1-en-3-yl diisopropylcarbamate(762261-99-4)
• EPA Substance Registry System: (3S,4R,5S)-5-(benzyloxy)-4-hydroxy-2-((trimethylsilyl)methyl)hex-1-en-3-yl diisopropylcarbamate(762261-99-4)

Safety Data

• Hazardous Substances Data: 762261-99-4(Hazardous Substances Data)

Upstream product

• 77287-11-7 methyl (S)-2-(benzyloxy)propanoate 
• 81445-44-5 (S)-2-(benzyloxy)propanal 

Downstream Products

• 854971-17-8 Acetic acid (2R,3S,4S,6R)-2-((S)-1-benzyloxy-ethyl)-3-diisopropylcarbamoyloxy-6-methoxy-tetrahydro-pyran-4-yl ester 
• 854971-27-0 Acetic acid (2R,3S,4S,6S)-2-((S)-1-benzyloxy-ethyl)-3-diisopropylcarbamoyloxy-6-methoxy-tetrahydro-pyran-4-yl ester 
• 854971-12-3 Diisopropyl-carbamic acid (2R,3S,4S,6R)-2-((S)-1-benzyloxy-ethyl)-4-hydroxy-6-methoxy-tetrahydro-pyran-3-yl ester 
• 854971-22-5 Diisopropyl-carbamic acid (2R,3S,4S,6S)-2-((S)-1-benzyloxy-ethyl)-4-hydroxy-6-methoxy-tetrahydro-pyran-3-yl ester 
• 854970-07-3 Diisopropyl-carbamic acid (2R,3S,6S)-2-((S)-1-benzyloxy-ethyl)-6-methoxy-4-methylene-tetrahydro-pyran-3-yl ester 
• 854970-02-8 Diisopropyl-carbamic acid (2R,3S,6R)-2-((S)-1-benzyloxy-ethyl)-6-methoxy-4-methylene-tetrahydro-pyran-3-yl ester 
• 762261-97-2 4-acetoxy-5-(benzyloxy)-2-((trimethylsilyl)methyl)hex-1-en-3-yl diisopropylcarbamate 

Relevant articles and documents

Stereoselective synthesis of functionalised triol units by SnCl4 promoted allylation of α-benzyloxyaldehydes: Crucial role of the stoichiometry of the Lewis acid

Enantiomerically pure syn-anti and syn-syn configured triol units are efficiently synthesized by the SnCl4 mediated allylation of chiral α-benzyloxyaldehydes with the uniquely functionalised allylstannane 9. Remarkably, the stereochemistry of t