65495-21-8

Basic information

• Product Name: N,N-dimethyl-3,4-dimethoxybenzylamine
• Synonyms: N,N-dimethyl-3,4-dimethoxybenzylamine
• CAS NO: 65495-21-8
• Molecular Weight: 195.261
• Mol File: 65495-21-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: N,N-dimethyl-3,4-dimethoxybenzylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethyl-3,4-dimethoxybenzylamine(65495-21-8)
• EPA Substance Registry System: N,N-dimethyl-3,4-dimethoxybenzylamine(65495-21-8)

Safety Data

• Hazardous Substances Data: 65495-21-8(Hazardous Substances Data)

Upstream product

• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 68-12-2 N,N-dimethyl-formamide 
• 124-40-3 dimethyl amine 
• 7306-46-9 4-chloromethyl-1,2-dimethoxy-benzene 
• 6967-45-9 3,4-dimethoxy-N,N-dimethylbenzamide 
• 106988-36-7 N,N-dimethyl(benzyl-d7)amine 
• 93-07-2 Veratric acid 
• 3535-37-3 3,4-dimethoxybenzoic acid chloride 
• 1008-89-5 2-phenylpyridine 
• 50-00-0 formaldehyd 
• 5763-61-1 3,4-dimethoxybenzylamine 
• 506-59-2 N,N-dimethylammonium chloride 

Downstream Products

• 93-03-8 (3,4-dimethoxyphenyl)methanol 
• 118-91-2 ortho-chlorobenzoic acid 
• 127-19-5 N,N-dimethyl acetamide 
• 53751-40-9 veratryl acetate 
• 101538-31-2 3,4-dimethoxybenzyl benzoate 
• 79809-14-6 N,N-dimethyl-3,4-dimethoxy-2-hydroxymethyl-benzylamine 
• 98352-19-3 Benzo[1,3]dioxol-5-yl-(6-dimethylaminomethyl-2,3-dimethoxy-phenyl)-methanol 
• 78792-50-4 6-Dimethylaminomethyl-2,3-dimethoxy-benzoic acid 
• 120-14-9 3,4-dimethoxy-benzaldehyde 
• 569-31-3 meconin 
• 65495-31-0 6-(chloromethyl)-2,3-dimethoxybenzoic acid ethyl ester 
• 78806-29-8 6-[(Ethoxycarbonyl-methyl-amino)-methyl]-2,3-dimethoxy-benzoic acid ethyl ester 
• 98352-17-1 (6-Dimethylaminomethyl-2,3-dimethoxy-phenyl)-phenyl-methanol 
• 98352-18-2 (3,4-Dimethoxy-phenyl)-(6-dimethylaminomethyl-2,3-dimethoxy-phenyl)-methanol 

Relevant articles and documents

Synthesis and oxidation-induced DNA cross-linking capabilities of bis(catechol) quaternary ammonium derivatives

A study was conducted to demonstrate the synthesis of a number of DNA crosslinking agents, such as bis(catechol) quaternary ammonium derives. It was found that these agents can crosslink DNA through an o-quinone intermediate, induced by oxidation. It was also found that these compounds are composed of two catechol monomers, acting as DNA cross-linking units and are joined by different linkers that act as DNA binding units. Positive charged linkers and quaternary ammonium derivatives were used in the study, to achieve high affinity to DNA. Aliphatic and aromatic chains were investigated, to determine their ability in performing favorable cross-linking reactions and to determine the relationship between agent flexibility and DNA cross-linking abilities.

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Discovery of dihydrooxazolo[2,3-: A] isoquinoliniums as highly specific inhibitors of hCE2

Human carboxylesterase 2 (hCE2) is one of the most abundant esterases distributed in human small intestine and colon, which participates in the hydrolysis of a variety of ester-bearing drugs and thereby affects the efficacy of these drugs. Herein, a new c