174623-83-7

Basic information

• Product Name: 13-Oxa-2,5,11-triazapentadecanoic acid, 3-(2-amino-2-oxoethyl)-14,14-dimethyl-4,12-dioxo-, phenylmethyl ester, (3S)-
• CAS NO: 174623-83-7
• Molecular Formula: C22H34N4O6
• Molecular Weight: 450.535
• Mol File: 174623-83-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 13-Oxa-2,5,11-triazapentadecanoic acid, 3-(2-amino-2-oxoethyl)-14,14-dimethyl-4,12-dioxo-, phenylmethyl ester, (3S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 13-Oxa-2,5,11-triazapentadecanoic acid, 3-(2-amino-2-oxoethyl)-14,14-dimethyl-4,12-dioxo-, phenylmethyl ester, (3S)-(174623-83-7)
• EPA Substance Registry System: 13-Oxa-2,5,11-triazapentadecanoic acid, 3-(2-amino-2-oxoethyl)-14,14-dimethyl-4,12-dioxo-, phenylmethyl ester, (3S)-(174623-83-7)

Safety Data

• Hazardous Substances Data: 174623-83-7(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 2304-96-3 N-benzyloxycarbonyl-L-asparagine 
• 462-94-2 1,5-diaminopentane 
• 3256-57-3 N-benzyloxycarbonyl-L-asparagine p-nitrophenyl ester 
• 51644-96-3 5-tert-butoxycarbonylamino-1-aminopentane 

Downstream Products

• 125739-24-4 (S)-N¹-(5-{3-[4-((S)-2-Amino-5-guanidino-pentanoylamino)-butylamino]-propionylamino}-pentyl)-2-[2-(2,4-dihydroxy-phenyl)-acetylamino]-succinamide; hydrochloride 
• 125718-78-7 (S)-N¹-(5-Amino-pentyl)-2-[2-(2,4-bis-benzyloxy-phenyl)-acetylamino]-succinamide; hydrochloride 
• 113954-15-7 (S)-N¹-(5-Amino-pentyl)-2-[2-(2,4-bis-benzyloxy-phenyl)-acetylamino]-succinamide 
• 125718-81-2 (5-{(S)-2-[2-(2,4-Bis-benzyloxy-phenyl)-acetylamino]-3-carbamoyl-propionylamino}-pentyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

Practical, convergent total synthesis of polyamine amide spider toxin NSTX-3

A practical, total synthesis of polyamine amide spider toxin NSTX-3, a potent glutamate receptor antagonist with potential as a neuroprotective agent, is reported. The unsymmetrical polyamine moiety was built by a conjugate addition to afford putreanine and regioselective acylation of L-asparaginyl-cadaverine.