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2-CYANO-ALPHA-CHLOROBENZALDOXIME is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

943518-99-8

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943518-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943518-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,5,1 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 943518-99:
(8*9)+(7*4)+(6*3)+(5*5)+(4*1)+(3*8)+(2*9)+(1*9)=198
198 % 10 = 8
So 943518-99-8 is a valid CAS Registry Number.

943518-99-8SDS

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 Benzenecarboximidoyl chloride, 2-cyano-N-hydroxy-

1.2 Other means of identification

Product number -
Other names 2-CYANO-ALPHA-CHLOROBENZALDOXIME

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:943518-99-8 SDS

943518-99-8Downstream Products

943518-99-8Relevant articles and documents

Synthesis of 3,5-Disubstituted isoxazoles containing privileged substructures with a diverse display of polar surface area

Kim, Mingi,Hwang, Yoon Soo,Cho, Wansang,Park, Seung Bum

, p. 407 - 413 (2017)

We designed and synthesized the molecular framework of 3,5-disubstituted isoxazoles containing privileged substructures with various substituents which uniquely display polar surface area in a diverse manner. A library of 3,5-disubstituted isoxazoles were systematically prepared via 1,3-dipolar cycloaddition of alkynes with nitrile oxides prepared by two complementary synthetic routes; method A utilized a halogenating agent with a base and method B utilized a hypervalent iodine reagent. Through the biological evaluation of corresponding isoxazoles via three independent phenotypic assays, the different pattern of biological activities was shown according to the type of privileged substructure and substituent. These results demonstrated the significance of molecular design via introducing privileged substructures and various substituents to make a diverse arrangement of polar surface area within a similar 3-dimensional molecular framework.

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