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2,4,5-trichloroimidazole is a chemical compound with the molecular formula C3HCl3N2, belonging to the imidazole family characterized by a five-membered heterocyclic ring with two nitrogen atoms. It is recognized for its strong Lewis acid properties, which make it a versatile compound in organic synthesis.

7682-38-4

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7682-38-4 Usage

Uses

Used in Pharmaceutical Industry:
2,4,5-trichloroimidazole is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a building block for developing new drugs with potential therapeutic applications.
Used in Agricultural Chemicals:
In the agricultural sector, 2,4,5-trichloroimidazole is utilized as an intermediate for the production of agricultural chemicals. Its chemical properties contribute to the development of effective pesticides and other agrochemicals designed to protect crops and enhance agricultural productivity.
Used in Dyes and Pigments Industry:
2,4,5-trichloroimidazole is employed as an intermediate in the synthesis of dyes and pigments. Its chemical composition plays a role in creating a range of colors used in various industries, including textiles, plastics, and printing inks.
Used in Organic Chemistry as a Reagent:
As a strong Lewis acid, 2,4,5-trichloroimidazole is used as a reagent in organic chemistry. It facilitates a variety of chemical reactions, making it an essential component in research and development laboratories.
Used in Polymer Production:
2,4,5-trichloroimidazole also serves as a building block in the production of different types of polymers. Its incorporation into polymer chemistry allows for the creation of materials with specific properties for use in various applications.
Safety Note:
Due to its potential for acute toxicity, 2,4,5-trichloroimidazole requires proper handling and disposal procedures to minimize its impact on human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 7682-38-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,8 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7682-38:
(6*7)+(5*6)+(4*8)+(3*2)+(2*3)+(1*8)=124
124 % 10 = 4
So 7682-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C3HCl3N2/c4-1-2(5)8-3(6)7-1/h(H,7,8)

7682-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,5-trichloro-1H-imidazole

1.2 Other means of identification

Product number -
Other names Imidazole,2,4,5-trichloro

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:7682-38-4 SDS

7682-38-4Relevant academic research and scientific papers

Chlorinated imidazole derivatives and a process for preparing them

-

, (2008/06/13)

Imidazole derivatives, useful as intermediates for making herbicides, having the formula STR1 wherein X is chlorine, lower alkyl mono- or polysubstituted by chlorine, or aryl which is optionally mono- or polysubstituted by halogen and/or lower alkyl and R1 and R2 are identical or different and are chlorine or phenyl optionally substituted by halogen and/or lower alkyl. The imidazole derivatives are prepared by converting an imidazole derivative having the formula STR2 wherein X' is hydrogen, lower alkyl or aryl optionally substituted by halogen atom and/or lower alkyl and R'1 and R'2 are identical and represent hydrogen and/or phenyl optionally substituted by halogen and/or lower alkyl By means of hydrogen chloride, in the absence of water, into the corresponding hydrochloride, subsequently reacting with hydrochloride with an excess of chlorine at elevated temperature.

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