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392-36-9

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392-36-9 Usage

Physical form

white crystalline solid

Uses

building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds; intermediate in the production of dyes, pigments, and fine chemicals

Properties

high thermal stability, resistance to oxidation, valuable reagent in organic synthesis

Potential applications

materials science, development of advanced polymers and high-performance materials

Check Digit Verification of cas no

The CAS Registry Mumber 392-36-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 392-36:
(5*3)+(4*9)+(3*2)+(2*3)+(1*6)=69
69 % 10 = 9
So 392-36-9 is a valid CAS Registry Number.

392-36-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-bis-trifluoromethyl-1(3)H-benzoimidazole

1.2 Other means of identification

Product number -
Other names 2,4-Bis-(trifluormethyl)-benzimidazol

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:392-36-9 SDS

392-36-9Downstream Products

392-36-9Relevant articles and documents

An efficient method to access 2-fluoroalkylbenzimidazoles by PIDA oxidation of amidines

Zhu, Jiangtao,Chen, Zixian,Xie, Haibo,Li, Shan,Wu, Yongming

, p. 134 - 138 (2012/02/05)

A mild and practical strategy for the synthesis of 2-bromodifluoromethyl (or trifluoromethyl)-1H-benzimidazoles via PIDA-mediated oxidative intramolecular cyclization of the fluorinated amidines is described. The approach has the advantages of superior yi

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