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2-(2,4-Dichloro-phenoxymethyl)-1H-benzoimidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

3156-21-6

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3156-21-6 Usage

Type of medication

Anthelmintic

Target animals

Dogs, cats, horses, and livestock

Mechanism of action

Interferes with the parasite's ability to absorb glucose

Result

Death of the parasite

Safety

Relatively safe for use in animals when administered at recommended dosages

Potential additional use

Anticancer properties in humans (as shown in recent studies)

Check Digit Verification of cas no

The CAS Registry Mumber 3156-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,5 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3156-21:
(6*3)+(5*1)+(4*5)+(3*6)+(2*2)+(1*1)=66
66 % 10 = 6
So 3156-21-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H10Cl2N2O/c15-9-5-6-13(10(16)7-9)19-8-14-17-11-3-1-2-4-12(11)18-14/h1-7H,8H2,(H,17,18)

3156-21-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2,4-Dichlorophenoxy)methyl]-1H-benzimidazole

1.2 Other means of identification

Product number -
Other names -

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:3156-21-6 SDS

3156-21-6Downstream Products

3156-21-6Relevant academic research and scientific papers

1-ethyl gallate-2-substituted phenoxymethyl benzimidazoles: Synthesis, molecular structure, antimicrobial activities and complex with Cr(III)

Zhao, Li,Qiu, Guirong,Wu, Jiacheng,Wang, Zhiyuan,Gu, Haibin

, p. 628 - 639 (2017/11/06)

Summary: The design of gallate and benzimidazole containing derivatives is expected to produce new bioactive molecules with multiple applications. Here the synthesis of eight novel benzimidazole compounds containing ethyl gallate and substituted phenoxyme

Discovery of some benzimidazole derivatives as a new agrochemical fungicides

Ibrahim, Nasser A.

experimental part, p. 823 - 836 (2012/07/27)

VARIOUSLY new substituted benzimidazole derivatives were synthesized with a wide range of suhstitucnis. Compounds were prepared by the reaction of 2-chloromethylbenzimidazole with different nitrogen, oxygen and sulfur nucleophiles as well as acetylacetone as an active methylene containing compound in organic solvent in the presence of hydrogen chloride acceptor. Most of the synthesized compounds were assayed for their fungicidal activity on three soil borne fungi. Some of the new synthesized compounds showed higher fungicidal activity than the standard fungicide Penycvcuron (Moncerene 25% WP).

A rapid and convenient synthesis of derivatives of imidazoles under Microwaveirradiation

Zhao, Na,Wang, Yu-Lu,Wang, Jin-Ye

, p. 535 - 538 (2007/10/03)

Anefficient and a quick microwave-assisted synthesis of benzimidazoles and trisubstituted imidazoles was developed. Three benzimidazoles were obtained as a result of the condensation of 1,2-phenylenediamine with carboxylic acids and acetoacetic ester without catalyst. A series of trisubstituted imidazoles were syn thesized by condensation of benzil, aromatical dehyde and ammonium acetate in the presence of glacial acetic acid.

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