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887-54-7

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887-54-7 Usage

Uses

The monoacidic metabolite of Dacthal, a pre-emergent herbicide.

Check Digit Verification of cas no

The CAS Registry Mumber 887-54-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 887-54:
(5*8)+(4*8)+(3*7)+(2*5)+(1*4)=107
107 % 10 = 7
So 887-54-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H4Cl4O4/c1-17-9(16)3-6(12)4(10)2(8(14)15)5(11)7(3)13/h1H3,(H,14,15)

887-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name chlorthal-monomethyl

1.2 Other means of identification

Product number -
Other names 2,3,5,6-tetrachloro-4-(methoxycarbonyl)benzoic 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:887-54-7 SDS

887-54-7Downstream Products

887-54-7Relevant articles and documents

2, 3, 5, 6 - Tetrachloro - 1, 4 - benzenedicarboxylic acid dimethyl manufacturing method

-

, (2021/04/29)

2, 3, 5, 6 - Tetrachloro - 1, 4 - benzenedicarboxylic acid dimethyl [to] horticultural herbicide useful in manufacturing, compared with conventional methods such as reducing environmentally harmful byproducts of hexachlorobenzene penta- chlorobenzene or content, can be efficiently manufactured in an industrial method. (I) formula [a]The manufacturing method of the compound represented, 2, 3, 5, 6 - tetrachloro - 1, 4 - benzenedicarboxylic acid (a), a ketone-based solvent in the presence of a hydrous alkali carbonate, prepared by reacting dimethyl sulfate, formula (I) compounds represented by the process to obtain the crystal, and (b) the crystal was washed with warm water of 30 a-°C 100, then further washed with an organic solvent comprising 30 a-°C 80, said method. [Drawing] no

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