61734-68-7

Basic information

• Product Name: Carbamic acid, (5,6-diamino-6-oxohexyl)-, phenylmethyl ester, (S)-
• CAS NO: 61734-68-7
• Molecular Formula: C14H21N3O3
• Molecular Weight: 279.339
• Mol File: 61734-68-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Carbamic acid, (5,6-diamino-6-oxohexyl)-, phenylmethyl ester, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamic acid, (5,6-diamino-6-oxohexyl)-, phenylmethyl ester, (S)-(61734-68-7)
• EPA Substance Registry System: Carbamic acid, (5,6-diamino-6-oxohexyl)-, phenylmethyl ester, (S)-(61734-68-7)

Safety Data

• Hazardous Substances Data: 61734-68-7(Hazardous Substances Data)

Upstream product

• 55592-81-9 N^ε-(benzyloxycarbonyl)-N^α-(tert-butoxycarbonyl)-L-lysinamide 
• 2389-46-0 N-α-tert-butyloxycarbonyl-N-ε-benzyloxycarbonyl-lysine p-nitrophenyl ester 
• 34404-36-9 Boc-Lys(Z)-OSu 
• 84890-96-0 C₂₄H₃₆N₂O₈ 
• 2389-45-9 Boc-Lys(Z)-OH 

Downstream Products

• 116019-49-9 Boc-Phe-D-Lys(Z)-NH₂ 
• 116019-55-7 C₆H₄-CH₂-CH₂-CO-D-Ala-Phe-D-Lys(Z)-NH₂ 
• 116019-58-0 C₆H₅-CH₂-CH₂-CO-D-Ala-Phe-D-Lys-NH₂ 
• 116019-67-1 H-D-Ala-Phe-D-Lys(Z)-NH₂ 
• 116019-51-3 Boc-D-Ala-Phe-D-Lys(Z)-NH₂ 
• 19653-71-5 (S)-3-Benzyloxycarbonylamino-N-((S)-5-benzyloxycarbonylamino-1-carbamoyl-pentyl)-succinamic acid benzyl ester 
• 50557-87-4 N^α-Acetyl-N^ε-benzyloxycarbonyl-L-lysinamid 
• 108713-08-2 Boc-Leu-Lys(Z)-NH₂ 
• 70117-59-8 benzyl ((S)-6-amino-5-((S)-2-((tert-butoxycarbonyl)amino)-3-phenylpropanamido)-6-oxohexyl)carbamate 
• 441024-82-4 Hexadecanoic acid (1R,2R)-1,2-bis-((S)-5-benzyloxycarbonylamino-1-carbamoyl-pentylcarbamoyl)-2-hexadecanoyloxy-ethyl ester 
• 917470-62-3 bNDI 
• 116019-64-8 benzyl ((S)-6-amino-5-((S)-2-amino-3-phenylpropanamido)-6-oxohexyl)carbamate 
• 108743-03-9 H-Orn-Phe-Phe-Gly-Leu-Lys-NH₂ 
• 108713-11-7 Boc-Orn(Boc)-Phe-Phe-Gly-Leu-Lys(Z)-NH₂ 

Relevant articles and documents

Solution-phase synthesis of a muramyl dipeptide analogue MDA

The solution-phase synthesis of a muramyl dipeptide (MDP) analogue of Nα-[4-chlorocinnamoyl-l-alanyl-d-isoglutaminyl]-l-lysine (MDA, 2) is reported that possesses the features of easy feasibility, safety and low cost in large scale of synthesis.

Structure-Activity Studies on the C-Terminal Hexapeptide of Substance P with Modifications at the Glutaminyl and Methioninyl Residues

Analogues of 6>-SP6-11 have been synthesized in which the SCH3 group of the Met11 side chain is replaced by other functional groups, such as (CH2)2NH2, COOH, CONH2, and COOR, which have basic, acidic, or neutral charac