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3-CHLOROMETHYL-4H-[1,2,4]TRIAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55928-92-2

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55928-92-2 Usage

General Description

3-Chloromethyl-4H-[1,2,4]triazole is a chemical compound that belongs to the class of triazoles. It is a white to off-white solid with the molecular formula C3H4ClN3. 3-CHLOROMETHYL-4H-[1,2,4]TRIAZOLE is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a fungicide and as a corrosion inhibitor in various industrial applications. Due to its versatile nature, 3-Chloromethyl-4H-[1,2,4]triazole has a wide range of potential uses in the chemical and pharmaceutical industries and is of interest to researchers and manufacturers alike.

Check Digit Verification of cas no

The CAS Registry Mumber 55928-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,9,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 55928-92:
(7*5)+(6*5)+(5*9)+(4*2)+(3*8)+(2*9)+(1*2)=162
162 % 10 = 2
So 55928-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C3H4ClN3/c4-1-3-5-2-6-7-3/h2H,1H2,(H,5,6,7)

55928-92-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(chloromethyl)-1H-1,2,4-triazole

1.2 Other means of identification

Product number -
Other names 3-chloromethyl-1,2,4-triazole

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:55928-92-2 SDS

55928-92-2Relevant academic research and scientific papers

Efficient syntheses of ω-chloro-, ω-imido- and ω-aminoalkyl-1,2,4-triazoles from N-acyl-formamidinium salts or N-acylformamides and hydrazines

Bechstein,Rumler,Liebscher

, p. 519 - 529 (2007/10/02)

ω-Halo and ω-amidoalkylcyanides 1 are transformed to ω-functionalized N-acylformamidinium salts 4 or formamide 6a by HCl catalyzed addition of chloromethylene iminium salts, derived from formamides 2 and POCl3. Advantageously, β-halo-propionyl-

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