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34662-36-7

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34662-36-7 Usage

Uses

3-Chloro-5-nitrobenzoic acid

Check Digit Verification of cas no

The CAS Registry Mumber 34662-36-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,6 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34662-36:
(7*3)+(6*4)+(5*6)+(4*6)+(3*2)+(2*3)+(1*6)=117
117 % 10 = 7
So 34662-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClNO4/c8-5-1-4(7(10)11)2-6(3-5)9(12)13/h1-3H,(H,10,11)

34662-36-7SDS

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 3-Chloro-5-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid, 3-chloro-5-nitro-

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:34662-36-7 SDS

34662-36-7Relevant articles and documents

The pyrazole derivative or its salt in a pharmaceutical composition containing them

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Paragraph 0081, (2017/01/26)

PROBLEM TO BE SOLVED: To provide a novel compound and a pharmaceutical composition useful for treatment and/or prevention of HIV virus infections.SOLUTION: Provided is a pyrazole derivative represented by the general formula (I) or a salt thereof (in the

Copper-catalyzed chlorination of functionalized arylboronic acids

Wu, Hong,Hynes Jr., John

supporting information; experimental part, p. 1192 - 1195 (2010/04/27)

"Chemical Equation Presented" A mild, efficient, Cu(I)-catalyzed method for the conversion of arylboronic acids to aryl chlorides Is reported. This method is particularly useful for the conversion of electron-deficient arylboronic acids to aryl chlorides, a transformation that is inefficient In the absence of Cu catalysis.

Macrolactams by engineered biosynthesis

-

, (2008/12/07)

Macrolactams are made by feeding aromatic amino acids as replacement starter units to a mutant strain of the geldanamycin-producing microorganism Streptomyces hygroscopicus var. geldanus NRRL 3602, wherein the gene cluster encoding enzymes for the biosynt

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