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1,2,4,5-Tetrachloro-3-fluorobenzene is a halogenated aromatic compound characterized by the presence of four chlorine atoms and one fluorine atom attached to a benzene ring. Specifically, the chlorine atoms are located at the 1, 2, 4, and 5 positions, while the fluorine atom is at the 3 position. This chemical is a colorless solid with a high melting point and low solubility in water. It is primarily used as an intermediate in the synthesis of various agrochemicals and pharmaceuticals, such as herbicides and insecticides. Due to its chemical structure, 1,2,4,5-tetrachloro-3-fluorobenzene exhibits significant stability and resistance to degradation, which can lead to potential environmental concerns if not properly managed.

319-97-1

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319-97-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 319-97-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,1 and 9 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 319-97:
(5*3)+(4*1)+(3*9)+(2*9)+(1*7)=71
71 % 10 = 1
So 319-97-1 is a valid CAS Registry Number.

319-97-1SDS

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 2,3,5,6-tetrachlorofluorobenzene

1.2 Other means of identification

Product number -
Other names 2,3,5,6-tetrachloro-fluorobenzene

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:319-97-1 SDS

319-97-1Relevant academic research and scientific papers

FLUORODENITRATIONS USING TETRABUTYLAMMONIUM FLUORIDE

Clark, James H.,Smith, David K.

, p. 2233 - 2236 (2007/10/02)

Fluoroaromatics are prepared in good yield under mild conditions using the tetrabutylammonium fluoride promoted fluorodenitration of nitroaromatics.

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