1268870-82-1

Basic information

• Product Name: (2S)-methyl 6-(benzylamino)-2-[(tert-butoxycarbonyl)amino]-5-hydroxyhexanoate
• Synonyms: (2S)-methyl 6-(benzylamino)-2-[(tert-butoxycarbonyl)amino]-5-hydroxyhexanoate
• CAS NO: 1268870-82-1
• Molecular Weight: 366.458
• Mol File: 1268870-82-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S)-methyl 6-(benzylamino)-2-[(tert-butoxycarbonyl)amino]-5-hydroxyhexanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-methyl 6-(benzylamino)-2-[(tert-butoxycarbonyl)amino]-5-hydroxyhexanoate(1268870-82-1)
• EPA Substance Registry System: (2S)-methyl 6-(benzylamino)-2-[(tert-butoxycarbonyl)amino]-5-hydroxyhexanoate(1268870-82-1)

Safety Data

• Hazardous Substances Data: 1268870-82-1(Hazardous Substances Data)

Downstream Products

• 1268870-84-3 (2S,5R)-2-[(tert-butoxycarbonyl)amino]-5-hydroxy-N-benzylcaprolactam 
• 1268870-85-4 (2S,5S)-2-[(tert-butoxycarbonyl)amino]-5-hydroxy-N-benzylcaprolactam 
• 144090-66-4 (2S,5S)-2-[(tert-butoxycarbonyl)amino]-5-hydroxycaprolactam 
• 270902-68-6 (3S, 6R)-3-(tert-butoxycarbonyl)aminohexahydro-6-hydroxy-2H-azepin-2-one 

Relevant articles and documents

Synthesis of 2-amino-5-hydroxycaprolactam derivatives mediated by E-selective olefination and asymmetric oxidation of the enol ether

The asymmetric synthesis of 2-amino-5-hydroxycaprolactam derivatives is essential for exploring the antitumor properties of ester-bearing bengamides. In this study, chiral caprolactam isomers were achieved on the basis of highly E-selective Wittig olefina