1904-62-7

Basic information

• Product Name: 2-DIMETHYLAMINOMETHYL-ANILINE
• Synonyms: 2-DIMETHYLAMINOMETHYL-ANILINE;Benzenemethanamine, 2-amino-N,N-dimethyl- (9CI);ar-Amino-N-benzyldimethylamine;N,N-Dimethyl-2-aminobenzenemethanamine;(2-aminobenzyl)dimethylamine(SALTDATA: 1.2HCl);BenzeneMethanaMine, 2-aMino-N,N-diMethyl-;2-[(Dimethylamino)methyl]aniline,tech
• CAS NO: 1904-62-7
• Molecular Formula: C₉H₁₄N₂
• Molecular Weight: 150.22
• Product Categories: AMINEPRIMARY
• Mol File: 1904-62-7.mol
• Article Data: 12

Chemical Properties

• Melting Point: 37-38 °C(Solv: hexane (110-54-3))
• Boiling Point: 232.072 °C at 760 mmHg
• Flash Point: 85.882 °C
• Appearance: /
• Density: 1.013 g/cm³
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• PKA: 8.62±0.28(Predicted)
• CAS DataBase Reference: 2-DIMETHYLAMINOMETHYL-ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-DIMETHYLAMINOMETHYL-ANILINE(1904-62-7)
• EPA Substance Registry System: 2-DIMETHYLAMINOMETHYL-ANILINE(1904-62-7)

Safety Data

• Hazardous Substances Data: 1904-62-7(Hazardous Substances Data)

Usage

General Description

2-Dimethylaminomethyl-aniline is a chemical compound often used in the industrial sector, particularly in the production of polymers, dyes, and pharmaceuticals. This organic compound, also known as N,N-Dimethylaminomethylbenzene, has the formula C9H13N and is known for its aromatic nature. It consists of a benzene ring substituted with a dimethylaminomethyl functional group. Handling of 2-Dimethylaminomethyl-aniline requires careful safety measures due to its potentially hazardous nature. It is typically a colorless to yellowish liquid and may pose health risks if ingested, inhaled, or come in contact with skin, eyes, or clothing. It may cause skin, eye, and respiratory irritation or severe burns.

Upstream product

• 103-83-3 N,N'-dimethylbenzylamine 
• 77422-70-9 azidomethyl phenyl sulphide 
• 55581-64-1 N,N-dimethyl-1-(2-nitrophenyl)methylamine 
• 612-23-7 2-nitrobenzyl chloride 
• 124-40-3 dimethyl amine 
• 552-89-6 2-nitro-benzaldehyde 
• 616-38-6 carbonic acid dimethyl ester 
• 4403-69-4 2-amino-1-benzylamine 
• 56222-15-2 N-(2-Dimethylaminomethyl-phenyl)-hydroxylamine 

Downstream Products

• 128457-33-0 N-(6,11-dihydrodibenzothiepin-11-yl)-2-(dimethylaminomethyl)aniline 
• 4282-72-8 N-(2-Dimethylaminomethyl-phenyl)-2-[(E)-hydroxyimino]-acetamide 
• 1264268-07-6 2-((dimethylamino)methyl)-N-(2-(diphenylphosphino)phenyl)aniline 
• 1264268-36-1 2-bromo-N-(2-((dimethylamino)methyl)phenyl)-aniline 

Relevant articles and documents

Exceptional Substrate Diversity in Oxygenation Reactions Catalyzed by a Bis(μ-oxo) Copper Complex

The enzyme tyrosinase contains a reactive side-on peroxo dicopper(II) center as catalytically active species in C?H oxygenation reactions. The tyrosinase activity of the isomeric bis(μ-oxo) dicopper(III) form has been discussed controversially. The synthesis of bis(μ-oxo) dicopper(III) species [Cu2(μ-O)2(L1)2](X)2 ([O1](X)2, X=PF6?, BF4?, OTf?, ClO4?), stabilized by the new hybrid guanidine ligand 2-{2-((dimethylamino)methyl)phenyl}-1,1,3,3-tetramethylguanidine (L1), and its characterization by UV/Vis, Raman, and XAS spectroscopy, as well as cryo-UHR-ESI mass spectrometry, is described. We highlight selective oxygenation of a plethora of phenolic substrates mediated by [O1](PF6)2, which results in mono- and bicyclic quinones and provides an attractive strategy for designing new phenazines. The selectivity is predicted by using the Fukui function, which is hereby introduced into tyrosinase model chemistry. Our bioinspired catalysis harnesses molecular dioxygen for organic transformations and achieves a substrate diversity reaching far beyond the scope of the enzyme.

Selective butyrylcholine esterase inhibitor or pharmaceutically acceptable salt thereof, and preparation method and application thereof

The invention discloses a selective butyrylcholine esterase inhibitor represented by a general formula (I) or a pharmaceutically acceptable salt thereof, and a preparation method and an application thereof. Butyrylcholine esterase inhibitory activity, sel

Hydrogenation of (N,N-disubstituted aminomethyl)nitrobenzenes to (N,N-disubstituted aminomethyl)anilines catalyzed by palladium-nickel bimetallic nanoparticles

Since palladium-catalysts have strong abilities for both hydrogenation of nitro-group and hydrogenolysis of benzylamine, they have a much lower chemoselectivity for the hydrogenation of (N,N-disubstituted aminomethyl)nitrobenzenes. In this article, component stable Pd-Ni bimetallic nanoparticles were prepared by simply heating RANEY-Ni and Na2PdCl4 together in water. They demonstrated novel synergistic effects when they were used as a bimetallic catalyst, by which a highly efficient and chemoselective hydrogenation of (N,N-disubstituted aminomethyl)nitrobenzenes to (N,N-disubstituted aminomethyl)anilines was achieved.