851909-06-3

Basic information

• Product Name: N-(N-(Boc)-L-homoallylglycyl)-N-(2-hydroxy-4-methoxybenzyl)-L-homoallylglycine methyl ester
• Synonyms: N-(N-(Boc)-L-homoallylglycyl)-N-(2-hydroxy-4-methoxybenzyl)-L-homoallylglycine methyl ester
• CAS NO: 851909-06-3
• Molecular Weight: 490.597
• Mol File: 851909-06-3.mol

Chemical Properties

• CAS DataBase Reference: N-(N-(Boc)-L-homoallylglycyl)-N-(2-hydroxy-4-methoxybenzyl)-L-homoallylglycine methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-(N-(Boc)-L-homoallylglycyl)-N-(2-hydroxy-4-methoxybenzyl)-L-homoallylglycine methyl ester(851909-06-3)
• EPA Substance Registry System: N-(N-(Boc)-L-homoallylglycyl)-N-(2-hydroxy-4-methoxybenzyl)-L-homoallylglycine methyl ester(851909-06-3)

Safety Data

• Hazardous Substances Data: 851909-06-3(Hazardous Substances Data)

Upstream product

• 410098-01-0 (2S)-2-aminohex-5-enoic acid methyl ester 
• 92136-57-7 (S)-2-tert-butoxycarbonylamino-hex-5-enoic acid methyl ester 
• 673-22-3 2-Hydroxy-4-methoxybenzaldehyde 
• 851909-12-1 methyl (2S)-2-[(2-hydroxy-6-methoxybenzyl)amino]hex-5-enoate 
• 208522-13-8 (S)-2-N-(tert-butoxycarbonyl)-2-amino-5-hexenoic acid 

Relevant articles and documents

Systematic study of the synthesis of macrocyclic dipeptide β-turn mimics possessing 8-, 9-, and 10- membered rings by ring-closing metathesis

A systematic study was performed to establish general synthesis protocols for forming enantiomerically pure macrocyclic dipeptide lactams. Focusing on macrocycles of 8-, 9-, and 10-membered rings, effective syntheses were achieved by a sequence featuring