160155-66-8

Basic information

• Product Name: 2-butylamino-4-diethylamino-6-(3-ethoxycarbonylaminomethylbenzylamino)-s-triazine
• Synonyms: 2-butylamino-4-diethylamino-6-(3-ethoxycarbonylaminomethylbenzylamino)-s-triazine
• CAS NO: 160155-66-8
• Molecular Weight: 429.566
• Mol File: 160155-66-8.mol

Chemical Properties

• CAS DataBase Reference: 2-butylamino-4-diethylamino-6-(3-ethoxycarbonylaminomethylbenzylamino)-s-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-butylamino-4-diethylamino-6-(3-ethoxycarbonylaminomethylbenzylamino)-s-triazine(160155-66-8)
• EPA Substance Registry System: 2-butylamino-4-diethylamino-6-(3-ethoxycarbonylaminomethylbenzylamino)-s-triazine(160155-66-8)

Safety Data

• Hazardous Substances Data: 160155-66-8(Hazardous Substances Data)

Upstream product

• 1722-19-6 2,4-dichloro-6-(diethylamino)-1,3,5-triazine 
• 1477-55-0 1,3-di(aminomethyl)benzene 
• 42829-57-2 2-butylamino-4-chloro-6-diethylamino-s-triazine 
• 263854-40-6 3-ethoxycarbonylaminomethylbenzylamine 
• 109-73-9 N-butylamine 
• 160155-65-7 {3-[(4-Chloro-6-diethylamino-[1,3,5]triazin-2-ylamino)-methyl]-benzyl}-carbamic acid ethyl ester 

Downstream Products

• 160155-67-9 2-[3-(aminomethyl)benzylamino]-4-butylamino-6-diethylamino-1,3,5-triazine 

Relevant articles and documents

Functionalized flavin receptors. Regulation of redox properties of 6- Azaflavin via hydrogen bondings with melamine derivatives bearing guanidinium ion(s) in organic solvents

Melamine derivatives bearing guanidinium ion(s) were synthesized as a flavin receptor using hydrogen bonds. The receptors bind 6-aza-10- dodecylisoalloxazine (6-azaflavin, 6-AzaFl) quite strongly via five or seven hydrogen bonds in CHCl3 or CHCl3-MeCN. Redox potentials of 6-AzaFl were considerably affected by hydrogen bondings of the receptors (positive shift: ΔE( 1/2 ) = 220-317 mV). Anionic semiquinone radical of 6-AzaFl was found to be stabilized by hydrogen bondings with a melamine derivative bearing an N- phenylguanidinium ion or two guanidinium ions. Effects of the hydrogen bondings on the oxidation activity of 6-AzaFl were kinetically investigated for the oxidation of N-benzyl-1,4-dihydronicotinamide (BNAH) and PhSH in CHCl3-MeCN under anaerobic conditions. It was found that the N(1)-hydrogen bonding facilitates a slight BNAH oxidation (3 - 104-fold).

A Flavin Receptor. Strong Binding Ability of a Melamine Derivative bearing a Guanidinium Ion for 6-Azaflavin: Five Hydrogen Bonds Formed in Chloroform

A melamine derivative bearing a guanidinium ion strongly binds 6-azaflavin via five hydrogen bonds with a binding constant of 140000 mol-1 dm3 in CHCl3.