143944-96-1

Upstream product

• 646-19-5 heptane-1,7-diamine 
• 143944-89-2 N-(tert-butyloxycarbonyl)-N-[(4-methylphenyl)sulfonyl]-4-chlorobutylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 18303-04-3 N-[(tert-butoxy)carbonyl]-4-methylbenzenesulfonamide 
• 278807-21-9 C₄₅H₅₂N₄O₈S₂ 
• 81505-98-8 N¹,N⁷-di(p-toluenesulfonyl)-1,7-diaminoheptane 
• 278807-22-0 C₃₁H₄₈N₄O₆S₂ 
• 143944-95-0 1,6,14,19-tetraaza-1,19-bis-t-butoxycarbonyl-1,6,14,19-tetra-p-toluenesulfonyl-nonadecane 

Downstream Products

• 277760-12-0 N¹,N⁵,N¹³,N¹⁷-tetra(p-toluenesulfonyl)-1,17-bis(ethylamino)-5,13-diazaheptadecane 

Relevant academic research and scientific papers

T7 RNA polymerase activation and improvement of the transcriptional sequencing by polyamines

We examined the possibility to improve the effectiveness of the in vitro transcription system using T7 RNA polymerase by coexistence with organic bases. The effect of the additives was evaluated by measuring the amount of RNA products in comparison with t

Use of the Mitsunobu reaction in the synthesis of polyamines

The Mitsunobu reaction has been used in the synthesis of polyamine analogues. The synthesis of the (R,R), (S,S) and meso-isomers of a tetraamine are described. The chemistry was used to synthesize a fluorinated polyamine analog and a hexaamine.

Polyamine phenols as radioprotective agents

The present invention relates to certain polyamine phenols which are useful as radioprotective agents.