121759-91-9

Basic information

• Product Name: Hexanoic acid, 6-[[1-oxo-6-[[(phenylmethoxy)carbonyl]amino]hexyl]amino]-, 4-nitrophenyl ester
• CAS NO: 121759-91-9
• Molecular Formula: C26H33N3O7
• Molecular Weight: 499.564
• Mol File: 121759-91-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Hexanoic acid, 6-[[1-oxo-6-[[(phenylmethoxy)carbonyl]amino]hexyl]amino]-, 4-nitrophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Hexanoic acid, 6-[[1-oxo-6-[[(phenylmethoxy)carbonyl]amino]hexyl]amino]-, 4-nitrophenyl ester(121759-91-9)
• EPA Substance Registry System: Hexanoic acid, 6-[[1-oxo-6-[[(phenylmethoxy)carbonyl]amino]hexyl]amino]-, 4-nitrophenyl ester(121759-91-9)

Safety Data

• Hazardous Substances Data: 121759-91-9(Hazardous Substances Data)

Upstream product

• 60-32-2 6-aminohexanoic acid 
• 53733-98-5 N-hydroxysuccinimide ester of 6-{[(benzyloxy)carbonyl]amino}hexanoic acid 
• 501-53-1 benzyl chloroformate 
• 1947-00-8 6-(benzyloxycarbonylamino)hexanoic acid 
• 100-02-7 4-nitro-phenol 
• 49701-55-5 13-benzyloxycarbonylamino-8-oxo-7-azatridecanoic acid 

Downstream Products

• 56403-09-9 1,8-diazacyclotetradecane-2,9-dione 

Relevant articles and documents

SYNTHESIS OF AZA-CROWN COMPOUNDS BY INTRAMOLECULAR CYCLIZATION OF ω-AMINO ACIDS

A method for the synthesis of aza-crown compounds by the intramolecular cyclization of ω-amino acids with subsequent reduction of the lactam to a macrocyclic amine was developed. 1,8-Diazacyclotetradecane and 1,8-dioxa-4,11-diazacyclotetradecane was synthesized in preparative yields.The structural assignments were made using the IR, 1H and 13C NMR, and mass spectra.