618436-57-0

Basic information

• Product Name: 5,10,15-tris(mesitylenesulfonyl)-5,10,15-triaza-1-heptadecylamine
• Synonyms: 5,10,15-tris(mesitylenesulfonyl)-5,10,15-triaza-1-heptadecylamine
• CAS NO: 618436-57-0
• Molecular Weight: 805.18
• Mol File: 618436-57-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5,10,15-tris(mesitylenesulfonyl)-5,10,15-triaza-1-heptadecylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 5,10,15-tris(mesitylenesulfonyl)-5,10,15-triaza-1-heptadecylamine(618436-57-0)
• EPA Substance Registry System: 5,10,15-tris(mesitylenesulfonyl)-5,10,15-triaza-1-heptadecylamine(618436-57-0)

Safety Data

• Hazardous Substances Data: 618436-57-0(Hazardous Substances Data)

Upstream product

• 304862-50-8 N¹,N⁴-bis(mesitylenesulfonyl)-N¹-(4-aminobutyl)-N⁴-ethylbutane-1,4-diamine 
• 304862-30-4 N-(3-aminobutyl)-N-ethylmesitylenesulfonamide 
• 189341-51-3 N¹,N⁴-bis(mesitylenesulfonyl)-N⁴-ethyl-1,4-diaminobutane 
• 151915-07-0 N-ethyl-(2-mesitylene)sulfonamide 
• 1351606-27-3 C₂₃H₂₈N₂O₄S 
• 773-64-8 2-mesitylenesulphonyl chloride 
• 161452-20-6 1,6,11-tris(mesitylenesulfonyl)-1,6,11-triazatridecane 
• 304863-09-0 3,8,13-tris(mesitylenesulfonyl)-3,8,13-triazahexadecylcyanide 

Downstream Products

• 304863-12-5 1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine 
• 1219742-41-2 C₆₂H₈₅N₅O₁₀S₄ 
• 304863-16-9 1,5,10,15,20-pentakis(mesitylenesulfonyl)-1,5,10,15,20-pentaazatricosane 
• 618436-58-1 5,10,15,20-tetrakis(mesitylenesulfonyl)-5,10,15,20-tetraaza-1-docosamine 
• 304863-14-7 3,8,13,18-tetrakis(mesitylenesulfonyl)-3,8,13,18-tetraazaheneicosanecyanide 

Relevant articles and documents

SYNTHESIS AND GROWTH REGULATORY ACTIVITY OF A PROTOTYPE MEMBER OF A NEW FAMILY OF AMlNOTHIOL RADIOPROTECTORS

The synthesis, growth inhibition and radioprotective activity of the PrC-210 aminothiol, 3-(methyl-amino)-2-((methylamino)methyl)propane-1-thiol, and its polyamine and thiolated polyamine progenitors are reported. All of the molecules significantly inhibi

Cyclopropane-containing polyamine analogues are efficient growth inhibitors of a human prostate tumor xenograft in nude mice

Polyamine analogues 7, 10, 18, 27, and 32 containing cyclopropane rings were obtained by chemical synthesis. Their antineoplastic activities were assessed against the cultured human prostate tumor cell lines DU-145, DuPro, and PC-3. Decamines 32 and 27 ex