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87974-51-4

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87974-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87974-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,7 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87974-51:
(7*8)+(6*7)+(5*9)+(4*7)+(3*4)+(2*5)+(1*1)=194
194 % 10 = 4
So 87974-51-4 is a valid CAS Registry Number.

87974-51-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-6-[1-(hydroxyamino)ethylidene]cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 2-hydroxy-5-chloroacetophenone oxime

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:87974-51-4 SDS

87974-51-4Relevant articles and documents

Amino sulfonyl compound, preparation method and uses thereof

-

Paragraph 0219; 0220, (2016/12/01)

The present invention relates to a new amino sulfonyl compound represented by a general formula I, or a tautomer, an enantiomer, a racemate or a pharmaceutically acceptable salt thereof, a preparation method, a pharmaceutical composition, and uses thereof, wherein the compound can be used for treatment of epilepsy, convulsion, obesity, and the like. The general formula I is defined in the specification.

Synthesis of 1,2-benzisoxazole 2-oxides

Kociolek, Martin G.,Hoermann, Olivia

body text, p. 2632 - 2638 (2012/08/08)

(Chemical Equation Presented) A series of 2-hydroxyaryl ketoximes were converted to the corresponding 1,2- benzisoxazole 2-oxides by treatment with iodobenzene diacetate (in acetic acid or methanol) or N-chlorosuccinimide in water. Both methods gave moderate to excellent yields for a variety of substituted oximes under mild conditions within short reaction times. The latter method has the advantages of an aqueous solvent and lack of halogenated organic by-products. Copyright Taylor & Francis Group, LLC.

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