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4-(2,4-Dichloro-m-toluoyl)-5-hydroxy-1,3-dimethyl-1H-pyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85163-32-2

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85163-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85163-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,1,6 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85163-32:
(7*8)+(6*5)+(5*1)+(4*6)+(3*3)+(2*3)+(1*2)=132
132 % 10 = 2
So 85163-32-2 is a valid CAS Registry Number.

85163-32-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(2,6-dichloro-3-methylbenzoyl)-2,5-dimethyl-1H-pyrazol-3-one

1.2 Other means of identification

Product number -
Other names 4-(2,4-Dichloro-m-toluoyl)-5-hydroxy-1,3-dimethyl-1H-pyrazole

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:85163-32-2 SDS

85163-32-2Downstream Products

85163-32-2Relevant academic research and scientific papers

Herbicidal 4-benzoyl-5-phenacyloxy-pyrazole derivatives, composition and method

-

, (2008/06/13)

A herbicidal compound having the following formula STR1 wherein n is 0 or 1; a herbicidal composition comprising said compound as an active ingredient; a process for producing said composition; and a herbicidal method employing said compound.

Process for producing 4-benzoylpyrazoles

-

, (2008/06/13)

4-Benzoyl-5-hydroxypyrazoles useful as herbicidal active ingredients, their intermediate or stabilizers against heat, oxidation or ultraviolet light are produced by a condensation of a pyrazolone, tetrachloromethane and a benzene compound in the presence of an aluminium halide, followed by a hydrolysis reaction with industrial advantages.

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