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17318-08-0

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17318-08-0 Usage

Chemical Properties

light yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 17318-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,1 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17318-08:
(7*1)+(6*7)+(5*3)+(4*1)+(3*8)+(2*0)+(1*8)=100
100 % 10 = 0
So 17318-08-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H2BrCl2F/c7-3-1-4(8)6(10)5(9)2-3/h1-2H

17318-08-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Bromo-1,3-dichloro-2-fluorobenzene

1.2 Other means of identification

Product number -
Other names 3,5-dichllor-4-fluoro-1-bromobenzene

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:17318-08-0 SDS

17318-08-0Relevant articles and documents

Preparation method of 3,5-dichloro-4-fluorobromobenzene compound

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Paragraph 0047-0052, (2020/12/14)

The invention relates to a preparation method of 3,5-dichloro-4-fluorobromobenzene. According to the preparation method, 2-fluoro-3-chloronitrobenzene is used as a starting raw material and subjectedto bromination, reduction and diazochlorination to synthesize 3,5-dichloro-4-fluorobromobenzene. The whole synthesis route of the method has the advantages of accessible raw materials, mild reaction conditions, environment friendliness, low equipment requirements and high product purity and yield.

Preparation method of 3,5-dichloro-4-fluorobromobenzene compound

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, (2020/12/15)

The invention relates to a preparation method of 3,5-dichloro-4-fluorobromobenzene, which comprises the steps of (1) reacting 2,4-dichloro-3-fluoroaniline with sulfuric acid in the presence of water and glacial acetic acid to obtain 2,4-dichloro-3-fluoroaniline sulfate; (2) adding bromine into the product mixture obtained in the step (1), then dropwise adding hydrogen peroxide, and reacting to obtain 2,4-dichloro-3-fluoro-6-bromoaniline sulfate; and (3) adding sodium hypophosphite and a catalyst copper salt into the product mixture obtained in the step (2), then dropwise adding sodium nitrite,and reacting to obtain 3,5-dichloro-4-fluorobromobenzene. The method is simple in process, low in cost, mild in condition, high in process safety and capable of effectively reducing the use amount ofbromine.

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