196704-28-6

Basic information

• Product Name: (3-Benzyloxycarbonylamino-propyl)-[3-(tert-butoxycarbonyl-{4-[tert-butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-amino)-propyl]-carbamic acid tert-butyl ester
• Synonyms: (3-Benzyloxycarbonylamino-propyl)-[3-(tert-butoxycarbonyl-{4-[tert-butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-amino)-propyl]-carbamic acid tert-butyl ester
• CAS NO: 196704-28-6
• Molecular Weight: 794.042
• Mol File: 196704-28-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (3-Benzyloxycarbonylamino-propyl)-[3-(tert-butoxycarbonyl-{4-[tert-butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-amino)-propyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3-Benzyloxycarbonylamino-propyl)-[3-(tert-butoxycarbonyl-{4-[tert-butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-amino)-propyl]-carbamic acid tert-butyl ester(196704-28-6)
• EPA Substance Registry System: (3-Benzyloxycarbonylamino-propyl)-[3-(tert-butoxycarbonyl-{4-[tert-butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-amino)-propyl]-carbamic acid tert-butyl ester(196704-28-6)

Safety Data

• Hazardous Substances Data: 196704-28-6(Hazardous Substances Data)

Upstream product

• 65564-05-8 3-[(benzyloxycarbonyl)amino]propanal 
• 114459-62-0 tri-Boc-spermine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 71-44-3 Spermine 
• 201984-66-9 1-trifluoroacetyl-5,10,14-tris-Boc-spermine 
• 202145-88-8 N-(3-((4-((3-aminopropyl)amino)butyl)amino)propyl)-2,2,2-trifluoroacetamide 
• 501-53-1 benzyl chloroformate 
• 34637-22-4 3-[(N-benzyloxycarbonyl)amino]propanol 
• 201984-76-1 N¹,N⁵,N¹⁰-tri-tert-butoxycarbonyl-N¹⁸-benzyloxycarbonyl-1,5,10,14,18-pentaazaoctadecane 

Downstream Products

• 128550-06-1 (N¹,N⁴,N⁹,N¹³-tetra-tert-butoxycarbonyl)-1,16-diamino-4,9,13-triazahexadecane 

Relevant articles and documents

A polyamine-modified near-infrared fluorescent probe for selective staining of live cancer cells

We report the synthesis of novel polyamine-modified near-infrared (NIR) probes, which show excellent water-solubility and good optical properties. One probe was taken up efficiently by living cancer cell lines whereas no staining of the non-cancer cells was observed.

Homologation of polyamines in the rapid synthesis of lipospermine conjugates and related lipoplexes

Lipopolyamine amides are useful cationic lipids, synthetic vectors for non-viral gene delivery. Desymmetrisation of readily available symmetrical polyamines is an important first step in the synthesis of such compounds. The application of trifluoroacetyl

Synthesis and pharmacological activity of philanthotoxin-343 analogs: Antagonists of ionotropic glutamate receptors

The synthesis of two classes of Philanthotoxin-343 analogs is described. Quantitative information on the antagonism of quisqualate-sensitive ionotropic glutamate receptors of insect muscle by these compounds is presented.