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36556-50-0

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36556-50-0 Usage

General Description

The chemical 2,3-Dichlorofluorobenzene is an organic compound with the molecular formula C6H3Cl2F. It is a colorless liquid that is used in the production of agrochemicals, pharmaceuticals, and other organic compounds. 2,3-Dichlorofluorobenzene is primarily used as an intermediate in the manufacture of pesticides, insecticides, and herbicides. It is also used as a solvent and as a starting material in the synthesis of other organic compounds. The chemical is known for its low solubility in water and its moderate toxicity, making it important to handle with proper precaution and safety measures. Its chemical structure consists of two chlorine atoms and one fluorine atom attached to a benzene ring, making it a halogenated aromatic compound.

Check Digit Verification of cas no

The CAS Registry Mumber 36556-50-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,5 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 36556-50:
(7*3)+(6*6)+(5*5)+(4*5)+(3*6)+(2*5)+(1*0)=130
130 % 10 = 0
So 36556-50-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl2F/c7-4-2-1-3-5(9)6(4)8/h1-3H

36556-50-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-Dichloro-3-fluorobenzene

1.2 Other means of identification

Product number -
Other names 2,3-Dichlorofluorobenzene

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:36556-50-0 SDS

36556-50-0Relevant articles and documents

Fluorination of aryl boronic acids using acetyl hypofluorite made directly from diluted fluorine

Vints, Inna,Gatenyo, Julia,Rozen, Shlomo

, p. 11794 - 11797 (2014/01/06)

Aryl boronic acids or pinacol esters containing EDG were converted in good yields and fast reactions to the corresponding aryl fluorides using the readily obtainable solutions of AcOF. In reactions with aryl boronic acids containing EWG at the para position, there are two competing forces: one directing the fluorination to take place ortho to the boronic acid and the other, toward an ipso substitution. With EWG meta to the boronic acid, substitution ipso to the boron moiety takes place in good yields.

A process for the preparation of o-chlorofluorobenzene

-

, (2008/06/13)

ο-Chlorofluorobenzene is prepared from 1,2,3-trichlorobenzene by partial fluorine exchange to a mixture of 2,6-dichlorofluorobenzene and 2,3-dichlorofluorobenzene followed by selective reduction to a mixture of fluorobenzene, ο-chlorofluorobenzene and 2,3-dichlorofluorobenzene. Each of the components of this latter mixture can be separated by a relatively easy distillation, and each has value as an intermediate in the manufacture of other valuable organic chemicals.

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