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163656-30-2

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163656-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163656-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,6,5 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 163656-30:
(8*1)+(7*6)+(6*3)+(5*6)+(4*5)+(3*6)+(2*3)+(1*0)=142
142 % 10 = 2
So 163656-30-2 is a valid CAS Registry Number.

163656-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-difluoro-3,5-dichlorobenzoic acid

1.2 Other means of identification

Product number -
Other names 3,5-dichloro-2,4-difluorobenzoic acid

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:163656-30-2 SDS

163656-30-2Downstream Products

163656-30-2Relevant articles and documents

An efficient synthesis of 2,4-difluoro-3,5-dichlorobenzoic acid

Zhou, Weiyou,Yu, Shuitao,Xia, Zhengjun,Zhang, Mingguang,Lin, Song,Chen, Zaixin

, p. 277 - 278 (2015)

2,4-Difluoro-3,5-dichlorobenzoic acid, as a key intermediate for preparing quinolone-3-carboxylic acids, was synthesised from the commercially available 2,4-difluoro-3-chlorobenzoic acid in excellent yield by a reaction sequence involving nitration, selec

2,3,4,5-tetrahalogenobenzene derivatives

-

, (2008/06/13)

2,3,4,5-trihalogenobenzene derivatives of the formula STR1 in which R is --COOH, --COCl, --COF, --CN, --CONH2, --CH2 OH, --CH2 Cl, --CHCl2, --CCl3 or --CHO, R1 is H, Cl or F, and R2 is Cl or F, it only being possible for R1 or R2 to be F, and processes for their preparation starting from benzonitriles reacted with potassium fluoride. The novel compounds are intermediates for antibacterials such as quinolone carboxylic acids.

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