184959-13-5

Basic information

• Product Name: 1H-Benzimidazole-2-ethanamine,1-methyl-(9CI)
• Synonyms: 1H-Benzimidazole-2-ethanamine,1-methyl-(9CI);2-(1-methyl-1H-benzimidazol-2-yl)ethanamine(SALTDATA: 2HCl);2-(1-Methyl-1H-benzo[d]iMidazol-2-yl)ethanaMine;[2-(1-Methyl-1H-benziMidazol-2-yl)ethyl]aMine dihydrochloride (SALTDATA: 2HCl);2-(1-methyl-1H-benzimidazol-2-yl)ethanamine hydrochloride;2-(1-methyl-2-benzimidazolyl)ethanamine;2-(1-methylbenzimidazol-2-yl)ethanamine;2-(1-methylbenzimidazol-2-yl)ethylamine
• CAS NO: 184959-13-5
• Molecular Formula: C10H13N3
• Molecular Weight: 175.234
• Product Categories: BENZIMIDAZOLE
• Mol File: 184959-13-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 354.4°C at 760 mmHg
• Flash Point: 168.1°C
• Appearance: /
• Density: 1.18g/cm³
• Vapor Pressure: 3.37E-05mmHg at 25°C
• Refractive Index: 1.624
• PKA: 9.39±0.10(Predicted)
• CAS DataBase Reference: 1H-Benzimidazole-2-ethanamine,1-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazole-2-ethanamine,1-methyl-(9CI)(184959-13-5)
• EPA Substance Registry System: 1H-Benzimidazole-2-ethanamine,1-methyl-(9CI)(184959-13-5)

Safety Data

• Hazardous Substances Data: 184959-13-5(Hazardous Substances Data)

Usage

General Description

1H-Benzimidazole-2-ethanamine, 1-methyl-(9CI) is a chemical compound with the molecular formula C10H12N2. It is also known as N-(1-Methyl-1H-benzimidazol-2-yl)ethanamine. 1H-Benzimidazole-2-ethanamine,1-methyl-(9CI) is a member of the benzimidazole class of chemicals, which are characterized by a benzene ring fused to an imidazole ring. It has potential applications in pharmaceutical research and development due to its structural properties and potential biological activity.1H-Benzimidazole-2-ethanamine, 1-methyl-(9CI) may have potential use as a precursor in the synthesis of various pharmaceuticals and as a target for drug design and discovery. Further research and investigation into its properties and potential applications are ongoing.

InChI:InChI=1/C10H13N3/c1-13-9-5-3-2-4-8(9)12-10(13)6-7-11/h2-5H,6-7,11H2,1H3

Upstream product

• 4760-34-3 N-methyl-1,2-phenylenediamine 
• 138078-14-5 2-(1-methyl-1H-benzo[d]imidazol-2-yl)ethanamine dihydrochloride 

Relevant articles and documents

Catalytic conversion of monophenols to ortho-quinones in a tyrosinase-like fashion: Towards more biomimetic and more efficient model systems

A new tyrosinase model based on the mononuclear copper(I) complex CuL bzm1 is synthesized and characterized. The ligand Lbzm1 of this system contains a combination of an imine and a benzimidazole function which renders the system more biomimetic in comparison to the recently published Lpy1 model of tyrosinase (M. Rolff, J. Schottenheim, G. Peters, F. Tuczek, Angew. Chem. Int. Ed. 2010, 122, 6583). As shown by UV/Vis and NMR spectroscopy, the CuLbzm1 complex catalytically mediates the conversion of the monophenol DTBP-H to the o-quinone DTBQ with a TON of 31. This reaction was also conducted in a stoichiometric fashion to get information about the involved intermediates and identify possible reasons for the observed increase in catalytic performance with respect to the Lpy1 system. DFT calculations were performed for the μ-catecholato dicopper intermediate, compound 4bzm. These calculations indicate a mixed valent Cu I-semiquinone-CuII structure, indicating that one-electron transfer from the monohydroxylated substrate to the copper centers has already occurred at this stage. Copyright