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392-61-0

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392-61-0 Usage

General Description

2,4-difluoro-1,3,5-trimethylbenzene is a chemical compound with the molecular formula C9H10F2. It is a colorless liquid with a strong odor, and it is primarily used as a solvent in various industrial applications. It is also used as a precursor in the production of other chemicals and in the synthesis of pharmaceuticals. Additionally, 2,4-difluoro-1,3,5-trimethylbenzene is utilized in the manufacturing of coatings and adhesives. However, it is important to handle this chemical with care as it can be harmful if inhaled, ingested, or comes into contact with the skin. Proper safety precautions should be followed when working with this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 392-61-0 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, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 392-61:
(5*3)+(4*9)+(3*2)+(2*6)+(1*1)=70
70 % 10 = 0
So 392-61-0 is a valid CAS Registry Number.

392-61-0SDS

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-difluoro-1,3,5-trimethylbenzene

1.2 Other means of identification

Product number -
Other names 2,4-difluoro-1,3,5-trimethyl-benzene

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:392-61-0 SDS

392-61-0Relevant articles and documents

Fluorination of aromatic compounds with N-fluorobenzenesulfonimide under solvent-free conditions

Andreev,Borodkin,Shubin

scheme or table, p. 1468 - 1473 (2010/03/24)

Reactions of N-fluorobenzenesulfonimide with methylbenzenes, phenols, and phenol ethers were studied under solvent-free conditions. The rate constant ratio for the reactions with mesitylene and durene indicates polar mechanism of the process. Solvent-free fluorination of aromatic compounds with N-fluorobenzenesulfonimide in some cases is more selective than reactions with other N-F reagents in a solvent.

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