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5,6-dichloro-1,2-dimethyl-1H-benzimidazole is a chemical compound with the molecular formula C9H8Cl2N2. It is a white crystalline solid that is soluble in organic solvents and has a molecular weight of 225.09 g/mol. 5,6-dichloro-1,2-dimethyl-1H-benzimidazole is known for its antifungal properties and is commonly used as an active ingredient in various pharmaceutical and agricultural products. It works by inhibiting the synthesis of ergosterol, an essential component of fungal cell membranes, thereby disrupting their growth and reproduction. Due to its effectiveness against a wide range of fungi, 5,6-dichloro-1,2-dimethyl-1H-benzimidazole is a valuable tool in the control of fungal infections in both humans and plants.

2818-64-6

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2818-64-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2818-64-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,1 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2818-64:
(6*2)+(5*8)+(4*1)+(3*8)+(2*6)+(1*4)=96
96 % 10 = 6
So 2818-64-6 is a valid CAS Registry Number.

2818-64-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,6-dichloro-1,2-dimethylbenzimidazole

1.2 Other means of identification

Product number -
Other names 5,6-dichloro-1,2-dimethyl-benzoimidazole

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:2818-64-6 SDS

2818-64-6Downstream Products

2818-64-6Relevant academic research and scientific papers

Combinatorial synthesis of benzimidazolium dyes and its diversity directed application toward GTP-selective fluorescent chemosensors

Wang, Shenliang,Chang, Young-Tae

, p. 10380 - 10381 (2006)

Highly selective fluorescence turn-on GTP sensor, GTP Green, was discovered by a diversity directed sensor approach, combined by solid-phase combinatorial synthesis of a benzimidazolium library and high-throughput screening. Copyright

Benzimidazolium dyes and their use as fluorescent chemosensors

-

Page/Page column 12, (2014/05/20)

The present invention is directed toward benzimidazolium dye compounds of formula (I) as follows: wherein, n is an integer from 2-10,m is an integer from 2-10,X1 and X2 are independently a halogen,Q is H or a resin, andR is (aromatic)o-(linker)p-with the linker being saturated or unsaturated C1-C5 hydrocarbons, each aromatic independently being a substituted or unsubstituted aromatic or heteroaromatic, o being 1 or 2, and p being 0 or 1. Methods of making and using these compounds are also disclosed.

BENZIMIDAZOLIUM DYES AND THEIR USE AS FLUORESCENT CHEMOSENSORS

-

, (2008/12/06)

The present invention is directed toward benzimidazolium dye compounds of formula (I) as follows: wherein, n is an integer from 2-10,m is an integer from 2-10,X1 and X2 are independently a halogen,Q is H or a resin, andR is (aromatic)o-(linker)p-with the linker being saturated or unsaturated C1-C5 hydrocarbons, each aromatic independently being a substituted or unsubstituted aromatic or heteroaromatic, o being 1 or 2, and p being 0 or 1. Methods of making and using these compounds are also disclosed.

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