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Phenol, 2-(1H-benzimidazol-2-yl)-6-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66892-99-7

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66892-99-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66892-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,9 and 2 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66892-99:
(7*6)+(6*6)+(5*8)+(4*9)+(3*2)+(2*9)+(1*9)=187
187 % 10 = 7
So 66892-99-7 is a valid CAS Registry Number.

66892-99-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(1,3-dihydrobenzimidazol-2-ylidene)-2-methylcyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 2-benzimidazol-2-yl-6-methylphenol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66892-99-7 SDS

66892-99-7Downstream Products

66892-99-7Relevant academic research and scientific papers

Synthesis and fungicidal activity of novel 6H-benzimidazo[1,2-c][1,3]benzoxazin-6-ones

Jiao, Yinchun,Ma, Caixia,Tan, Yuhuan,Tang, Zilong

, p. 581 - 587 (2021/06/16)

[Figure not available: see fulltext.] A series of 6H-benzimidazo[1,2-c][1,3]benzoxazin-6-one derivatives were synthesized in moderate to good yield by reaction of 2-(1H-benzimidazol-2-yl)phenols with triphosgene, and the structures of the target compounds

The ninhydrin core as carbonyl source to access 2-(2′-hydroxyaryl)benzimidazoles exploiting the ortho selectivity of ninhydrin-phenol adducts

Das, Suven,Maity, Suvendu,Ghosh, Prasanta,Dutta, Arpita

, p. 2862 - 2872 (2021/08/13)

Although ninhydrin is an essential analytical tool in biochemical and forensic sciences, for the past several years, it has been employed as efficient building block for diverse organic scaffolds. In the present work, the ortho selectivity of ninhydrin-phenol adducts has been exploited to obtain 2-(2′-hydroxyaryl)benzimidazoles which are well known excited state intramolecular proton transfer (ESIPT) fluorophores. Under acidic condition, 3-(2-hydroxyaroyl)isoindolin-1-one intermediate generated in situ from ninhydrin-phenol adducts was treated with o-phenylenediamine resulting benzimidazole scaffolds via a two-step one pot strategy.

Small heterocycles as highly luminescent building blocks in the solid state for organic synthesis

Da Silveira Santos, Fabiano,Medeiros, Natália Goedtel,Affeldt, Ricardo Ferreira,Da Costa Duarte, Rodrigo,Moura, Sidnei,Rodembusch, Fabiano Severo

, p. 2785 - 2791 (2016/03/22)

New photoactive mono-formylated benzoxazole derivatives were obtained as stable solids with excellent yields through a Duff functionalization protocol using a simple synthetic methodology. Despite several attempts to obtain the desired formyl compounds th

Spectral characterization and antibacterial effect of 2-Methyl-6-(5-H/Me/ Cl/NO2-1H-benzimidazol-2-yl)-phenols and some transition metal complexes

Tavman, Aydin,Ikiz, Serkan,Bagcigil, A. Funda,?zgür, N. Yakut,Ak, Seyyal

experimental part, p. 215 - 222 (2010/07/04)

2-Methyl-6-(5-H/methyl/chloro/nitro-1H-benzimidazol-2-yl)-phenols (HL x: x = 1-4) ligands and HL1 complexes with Fe(NO 3)3, Cu(NO3)2, AgNO3, Zn(NO3)2 have b

Synthesis of Some Imidazole- and Pyrazole- Derived Chelating Agents

Addison, Anthony W.,Burke, Philip J.

, p. 803 - 805 (2007/10/02)

Procedures involving condensation of o-phenylenediamines with carboxylic acids, and reaction of bifunctional alkyl halides with bifunctional nucleophiles are described.Syntheses are reported of 2,6-bis(2-benzimidazyl)-pyridine, 1,3-bis(2-benzimidazyl)-2-thiapropane, 1,7-bis(2-benzimidazyl)-2,6-dithiaheptane, 2-hydroxymethyl-5,6-dimethylbenzimidazole, 2-chloromethyl-5,6-dimethylbenzimidazole hydrochloride, 1,7-bis(5,6-dimethyl-2-benzimidazyl)-2,6-dithiaheptane, 3,6-bis(1-pyrazolyl)pyridazine, 2-(2-hydroxy-3-methylphenyl)benzimidazole, 2-(2-hydroxyphenyl)benzimidazole, 5-(2-hydroxyphenyl)-3-methyl-1-phenylpyrazole, 3(5)-(2-hydroxyphenyl)-5(3)-methylpyrazole, 3(5)-(2-hydroxyphenyl)-5(3)-phenylpyrazole, and 1,3-bis((5-methylpyridyl)imino)isoindoline.

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