304862-50-8

Basic information

• Product Name: N¹,N⁴-bis(mesitylenesulfonyl)-N¹-(4-aminobutyl)-N⁴-ethylbutane-1,4-diamine
• Synonyms: N¹,N⁴-bis(mesitylenesulfonyl)-N¹-(4-aminobutyl)-N⁴-ethylbutane-1,4-diamine
• CAS NO: 304862-50-8
• Molecular Weight: 551.815
• Mol File: 304862-50-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N¹,N⁴-bis(mesitylenesulfonyl)-N¹-(4-aminobutyl)-N⁴-ethylbutane-1,4-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N¹,N⁴-bis(mesitylenesulfonyl)-N¹-(4-aminobutyl)-N⁴-ethylbutane-1,4-diamine(304862-50-8)
• EPA Substance Registry System: N¹,N⁴-bis(mesitylenesulfonyl)-N¹-(4-aminobutyl)-N⁴-ethylbutane-1,4-diamine(304862-50-8)

Safety Data

• Hazardous Substances Data: 304862-50-8(Hazardous Substances Data)

Upstream product

• 1351606-27-3 C₂₃H₂₈N₂O₄S 
• 189341-51-3 N¹,N⁴-bis(mesitylenesulfonyl)-N⁴-ethyl-1,4-diaminobutane 
• 151915-07-0 N-ethyl-(2-mesitylene)sulfonamide 
• 773-64-8 2-mesitylenesulphonyl chloride 
• 304862-48-4 N³,N⁸-bis(mesitylenesulfonyl)-3,8-diazalauronitrile 
• 304862-30-4 N-(3-aminobutyl)-N-ethylmesitylenesulfonamide 
• 304862-28-0 N-ethyl-N-(3-cyanobutyl)mesitylenesulfonamide 

Downstream Products

• 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 
• 304863-12-5 1,6,11,16-tetrakis(mesitylenesulfonyl)-6,11,16-tetraaza-1-heptadecylamine 
• 618436-57-0 5,10,15-tris(mesitylenesulfonyl)-5,10,15-triaza-1-heptadecylamine 
• 1219742-41-2 C₆₂H₈₅N₅O₁₀S₄ 
• 304862-57-5 N³,N⁸,N¹³,N¹⁸,N²³-pentakis(mesitylenesulfonyl)-3,8,13,18,23-pentaaza-(20Z)-pentacosene 
• 304862-55-3 N³,N⁸,N¹³,N¹⁸,N²³-pentakis(mesitylenesulfonyl)-3,8,13,18,23-pentaaza-(15Z,20Z)-pentacosadiene 
• 304862-59-7 N³,N⁸,N¹³,N¹⁸,N²³-pentakis(mesityelenesulfonyl)-3,8,13,18,23-pentaaza-(15Z)-pentacosene 
• 161452-20-6 1,6,11-tris(mesitylenesulfonyl)-1,6,11-triazatridecane 

Relevant articles and documents

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Synthesis and evaluation of unsymmetrical polyamine derivatives as antitumor agents

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