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2-Ethyl-5,6-dimethyl-1H-benzoimidazole is an organic compound with the molecular formula C11H14N2. It is a derivative of benzoimidazole, a heterocyclic aromatic organic compound containing a benzene ring fused to an imidazole ring. The structure of 2-ethyl-5,6-dimethyl-1H-benzoimidazole is characterized by an ethyl group at the 2nd position, and two methyl groups at the 5th and 6th positions of the benzene ring. 2-ethyl-5,6-dimethyl-1H-benzoimidazole is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a pesticide. It is also used as an intermediate in the synthesis of various chemical compounds. Due to its specific structure, it exhibits unique chemical properties and reactivity, making it a valuable component in the development of new drugs and other chemical products.

4887-89-2

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4887-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4887-89-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4887-89:
(6*4)+(5*8)+(4*8)+(3*7)+(2*8)+(1*9)=142
142 % 10 = 2
So 4887-89-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H14N2/c1-4-11-12-9-5-7(2)8(3)6-10(9)13-11/h5-6H,4H2,1-3H3,(H,12,13)

4887-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethyl-5,6-dimethyl-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names 5,6-dimethyl-2-ethylbenzimidazole

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:4887-89-2 SDS

4887-89-2Downstream Products

4887-89-2Relevant academic research and scientific papers

A novel ternary GO@SiO2-HPW nanocomposite as an efficient heterogeneous catalyst for the synthesis of benzazoles in aqueous media

Habibzadeh, Setareh,Firouzzadeh Pasha, Ghasem,Tajbakhsh, Mahmood,Amiri Andi, Nasim,Alaee, Ehsan

, p. 934 - 944 (2019/06/13)

A new solid acid catalyst, consisting of 12-phosphotungstic heteropoly acid (HPW) supported on graphene oxide/silica nanocomposite (GO@SiO2), has been developed via immobilizing HPW onto an amine-functionalized GO/SiO2 surface through coordination interaction (GO@SiO2-HPW). The GO@SiO2-HPW nanocomposite was characterized by Fourier transform infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and powder X-ray diffraction (XRD). The prepared nanocomposite could be dispersed homogeneously in water and further used as a heterogeneous, reusable, and efficient catalyst for the synthesis of benzimidazoles and benzothiazoles by the reaction of 1,2-phenelynediamine or 2-aminothiophenol with different aldehydes.

Water-mediated synthesis of 2-substituted benzimidazoles by boric acid and glycerol

Mukhopadhyay, Chhanda,Tapaswi, Pradip Kumar,Butcher, Ray J.

experimental part, p. 140 - 144 (2009/08/15)

A very simple, mild, and highly efficient green catalyst has been developed for the synthesis of 2-substituted benzimidazoles by treatment of substituted ortho-phenylenediamines and aldehydes in water at 80C in the presence of boric acid (5 mol-%) and glycerol (0.05 mL). This methodology has been standardized on 55 substrates, and nine new compounds have been synthesized.

A highly effective sulfamic acid/methanol catalytic system for the synthesis of benzimidazole derivatives at room temperature

Zhang, Zhan-Hui,Li, Tong-Shuang,Li, Jian-Jiong

, p. 89 - 94 (2007/10/03)

Sulfamic acid/methanol was found to be an efficient catalytic system for the synthesis of benzimidazole compounds through the condensation of o-phenylenediamine with orthoester in high yields at room temperature.

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