141949-61-3

Basic information

• Product Name: (1'R,2'R)-N-<2-(2'-Acetylaminocyclohexyloxy)acetyl>-L-alanyl-D-glutamic acid
• CAS NO: 141949-61-3
• Molecular Weight: 415.444
• Mol File: 141949-61-3.mol

Chemical Properties

• CAS DataBase Reference: (1'R,2'R)-N-<2-(2'-Acetylaminocyclohexyloxy)acetyl>-L-alanyl-D-glutamic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1'R,2'R)-N-<2-(2'-Acetylaminocyclohexyloxy)acetyl>-L-alanyl-D-glutamic acid(141949-61-3)
• EPA Substance Registry System: (1'R,2'R)-N-<2-(2'-Acetylaminocyclohexyloxy)acetyl>-L-alanyl-D-glutamic acid(141949-61-3)

Safety Data

• Hazardous Substances Data: 141949-61-3(Hazardous Substances Data)

Upstream product

• 142034-79-5 (1R,2R)-2-Carbomethoxycyclohexylammonium chloride 
• 142034-81-9 (1'R,2'R)-2-(2'-Acetylaminocyclohexyloxy)acetic acid 
• 142034-76-2 2-chloro-N-[trans-(1,2)-2-hydroxycyclohexyl]acetamide 
• 142034-77-3 (trans-4a,8a)-hexahydro-2H-1,4-benzoxazin-3(4H)-one 
• 134961-98-1 trans-2-(2'-acetylaminocyclohexyloxy)acetic acid 
• 127958-79-6 rac-trans-2-(2'-Aminocyclohexyloxy)acetic acid 
• 931-15-7 (1R,2R)-2-aminocyclohexanol 
• 141949-60-2 (1'R,2'R)-Dibenzyl-N-<2-(2'-acetylaminocyclohexyloxy)acetyl>-L-alanyl-D-glutamate 
• 142034-80-8 (1S,2S)-2-Carbomethoxycyclohexylammonium chloride 
• 142034-82-0 (1'S,2'S)-2-(2'-Acetylaminocyclohexyloxy)acetic acid 
• 142034-75-1 (1'S,2'S)-N-(2'-Hydroxycyclohexyl)-2-chloroacetamide 
• 142034-78-4 (4aS,8aS)-Octahydro-2H-1,4-benzoxazin-3-one 
• 931-15-7 (1S,2S)-trans-2-aminocyclohexanol 
• 141949-60-2 (1'S,2'S)-Dibenzyl-N-<2-(2'-acetylaminocyclohexyloxy)acetyl>-L-alanyl-D-glutamate 

Relevant articles and documents

Preparation of diastereomerically pure immunologically active carbocyclic nor-muramyldipeptide analogues

The preparation of diastereomerically pure immunologically active carbocyclic nor-muramyldipeptide analogues (1'R,2'R)-/(1'S,2'S)-N-[2-(2'-acetylaminocyclohexyloxy)acetyl]-L- alanyl-D-isoglutamine and (1'R,2'R)-/(1'S,2'S)-N-[2-(2'-acetylaminocyclohexyloxy)acetyl]-L- alanyl-D-glutamic acid is described. The title compounds were synthesized using two independent synthetic routes from racemic trans-2-azidocyclohexanol and (1R,2R)-/(1S,2S)-2-aminocyclohexanol, respectively.