914618-54-5

Basic information

• Product Name: (1R,2S)-1,2-bis(benzyloxy)-1-p-methoxyphenylbut-3-ene
• Synonyms: (1R,2S)-1,2-bis(benzyloxy)-1-p-methoxyphenylbut-3-ene
• CAS NO: 914618-54-5
• Molecular Weight: 374.48
• Mol File: 914618-54-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (1R,2S)-1,2-bis(benzyloxy)-1-p-methoxyphenylbut-3-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-1,2-bis(benzyloxy)-1-p-methoxyphenylbut-3-ene(914618-54-5)
• EPA Substance Registry System: (1R,2S)-1,2-bis(benzyloxy)-1-p-methoxyphenylbut-3-ene(914618-54-5)

Safety Data

• Hazardous Substances Data: 914618-54-5(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 100-39-0 benzyl bromide 
• 106948-24-7 (allyl)(diisopropylamino)dimethylsilane 
• 865565-60-2 (1R,2S)-1-(p-methoxyphenyl)but-3-ene-1,2-diol 

Downstream Products

• 914618-53-4 (1R,2S)-benzyl N-(2-benzyloxy-1-p-methoxyphenylbut-3-enyl)carbamate 
• 914618-62-5 3-benzoyloxy-piperidine-1,2-dicarboxylic acid 1-benzyl ester 
• 933471-53-5 (2R,3S)-3-benzyloxycarbonyl-2-p-methoxyphenylpiperidine 
• 914618-56-7 (1R,2S)-benzyl N-allyl-N-(2-benzyloxy-1-p-methoxyphenylbut-3-enyl)carbamate 
• 914618-52-3 (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)piperidine 
• 914618-57-8 (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)-1,2,3,6-tetrahydropyridine 
• 914618-58-9 (2R,3S)-1-benzyloxycarbonyl-(3-benzoyloxy-2-hydroxymethyl)piperidine 
• 952143-95-2 (2S,3S,6S)-methyl 3-(benzyloxy)-6-dodecylpiperidine-2-carboxylate 
• 952143-98-5 (2S,3S)-2-(benzyloxycarbonylamino)-1-methoxy-1,6-dioxooctadecan-3-yl benzoate 
• 952143-97-4 benzyl (1R,2S)-2-(benzyloxy)-1-(4-methoxyphenyl)-5-oxoheptadecyl carbamate 
• 952143-96-3 benzyl (1R,2S)-2-(benzyloxy)-1-(4-methoxyphenyl)-5-oxoheptadecen-(3E)-enyl carbamate 

Relevant articles and documents

Stereoselective synthesis of D-1-deoxynojirimycin and its stereoisomers

A stereoselective synthesis of D-l-deoxynojirimycin (1), D-1-deoxymannojirimycin (2), and D-1-deoxyallonojirimycin (3) was achieved via the regioselective and diastereoselective amination of anti-l,2-dibenzyl ether using chlorosulfonyl isocyanate (CSI), ring-closing metathesis, diastereoselective dihydroxylation, and the regioselective stereochemical inversion of the resulting diol.

An efficient stereoselective synthesis of (+)-deoxoprosophylline

An efficient stereoselective synthesis of (+)-deoxoprosophylline from readily available p-anisaldehyde is described. Key steps in the synthesis include the stereoselective amination of anti-1,2-dibenzyl ether using chlorosulfonyl isocyanate, intermolecula