201984-76-1

Basic information

• Product Name: N¹,N⁵,N¹⁰-tri-tert-butoxycarbonyl-N¹⁸-benzyloxycarbonyl-1,5,10,14,18-pentaazaoctadecane
• Synonyms: N¹,N⁵,N¹⁰-tri-tert-butoxycarbonyl-N¹⁸-benzyloxycarbonyl-1,5,10,14,18-pentaazaoctadecane
• CAS NO: 201984-76-1
• Molecular Weight: 693.925
• Mol File: 201984-76-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N¹,N⁵,N¹⁰-tri-tert-butoxycarbonyl-N¹⁸-benzyloxycarbonyl-1,5,10,14,18-pentaazaoctadecane(CAS DataBase Reference)
• NIST Chemistry Reference: N¹,N⁵,N¹⁰-tri-tert-butoxycarbonyl-N¹⁸-benzyloxycarbonyl-1,5,10,14,18-pentaazaoctadecane(201984-76-1)
• EPA Substance Registry System: N¹,N⁵,N¹⁰-tri-tert-butoxycarbonyl-N¹⁸-benzyloxycarbonyl-1,5,10,14,18-pentaazaoctadecane(201984-76-1)

Safety Data

• Hazardous Substances Data: 201984-76-1(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 71-44-3 Spermine 
• 501-53-1 benzyl chloroformate 
• 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 
• 34637-22-4 3-[(N-benzyloxycarbonyl)amino]propanol 

Downstream Products

• 128550-06-1 (N¹,N⁴,N⁹,N¹³-tetra-tert-butoxycarbonyl)-1,16-diamino-4,9,13-triazahexadecane 
• 196704-28-6 (3-Benzyloxycarbonylamino-propyl)-[3-(tert-butoxycarbonyl-{4-[tert-butoxycarbonyl-(3-tert-butoxycarbonylamino-propyl)-amino]-butyl}-amino)-propyl]-carbamic acid tert-butyl ester 

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