914618-57-8

Basic information

• Product Name: (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)-1,2,3,6-tetrahydropyridine
• Synonyms: (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)-1,2,3,6-tetrahydropyridine
• CAS NO: 914618-57-8
• Molecular Weight: 429.516
• Mol File: 914618-57-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)-1,2,3,6-tetrahydropyridine(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)-1,2,3,6-tetrahydropyridine(914618-57-8)
• EPA Substance Registry System: (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)-1,2,3,6-tetrahydropyridine(914618-57-8)

Safety Data

• Hazardous Substances Data: 914618-57-8(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 914618-53-4 (1R,2S)-benzyl N-(2-benzyloxy-1-p-methoxyphenylbut-3-enyl)carbamate 
• 914618-54-5 (1R,2S)-1,2-bis(benzyloxy)-1-p-methoxyphenylbut-3-ene 
• 865565-60-2 (1R,2S)-1-(p-methoxyphenyl)but-3-ene-1,2-diol 
• 106-95-6 allyl bromide 
• 914618-56-7 (1R,2S)-benzyl N-allyl-N-(2-benzyloxy-1-p-methoxyphenylbut-3-enyl)carbamate 

Downstream Products

• 950823-73-1 (2R,3R,4S,5S)-3-benzyloxy-1-benzyloxycarbonyl-4,5-dihydroxy-2-(p-methoxyphenyl)piperidine 
• 914618-58-9 (2R,3S)-1-benzyloxycarbonyl-(3-benzoyloxy-2-hydroxymethyl)piperidine 
• 933471-53-5 (2R,3S)-3-benzyloxycarbonyl-2-p-methoxyphenylpiperidine 
• 914618-62-5 3-benzoyloxy-piperidine-1,2-dicarboxylic acid 1-benzyl ester 
• 208649-02-9 (2S,3S)-3-hydroxypipecolic acid 
• 914618-52-3 (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)piperidine 

Relevant articles and documents

Synthesis and conformational analysis of 3-hydroxypipecolic acid analogs via CSI-mediated stereoselective amination

A short and efficient stereoselective synthetic approach toward substituted piperidines, involving (2S,3S)-3-hydroxypipecolic acid 1, (2R,3S)-3-hydroxypipecolic acid 3, and their acid-reduced analogs 2 and 4, has been developed. The requisite anti- and sy

An efficient stereoselective synthesis of (2S,3S)-3-hydroxypipecolic acid using chlorosulfonyl isocyanate

An efficient stereoselective syntheses of (2S,3S)-3-hydroxypipecolic acid and (2R,3S)-2-hydroxymethylpiperidin-3-ol were achieved from p-anisaldehyde via the regioselective and diastereoselective introduction of an N-protected amine group using chlorosulf