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N-[4-Chlorophenylsulfonyl]benzenecarboxamidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14067-79-9

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14067-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14067-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,6 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14067-79:
(7*1)+(6*4)+(5*0)+(4*6)+(3*7)+(2*7)+(1*9)=99
99 % 10 = 9
So 14067-79-9 is a valid CAS Registry Number.

14067-79-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-(4-chlorophenyl)sulfonylbenzenecarboximidamide

1.2 Other means of identification

Product number -
Other names -

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:14067-79-9 SDS

14067-79-9Relevant academic research and scientific papers

Activated sterically strained C=N bond in N-substituted p-quinonemono- and -diimines: X. Reactions of N-[N-arylsulfonylbenz(acet)imidoyl]-3,5-dimethyl-1,4-benzoquinonimines with alcohols

Avdeenko,Marchenko

, p. 1587 - 1591 (2007/10/03)

N-[N-Arylsulfonylbenz(acet)imidoyl]-3,5-dimethyl-1,4-benzoquinonimines react with alcohols to give the corresponding adducts at the activated C=N bond. The adducts lose alcohol molecule on heating to afford initial quinonimines. Hydrolysis of the title co

N2-(ARYLSULFONYL)ARYLAMIDINES. SYNTHESIS AND PROPERTIES OF N2-(ARYLSULFONYL)ARYLAMIDINES AND THEIR N1-ACYL DERIVATIVES

Dubina, V. L.,Shebitchenko, L. N.,Pedan, V. P.,Yukhno, A. G.,Skripets, V. I.

, p. 691 - 696 (2007/10/02)

The reaction of carboxylic acid chlorides with N2-(arylsulfonyl)benzamidines was investigated.Conditions were found for the production of N2-arylsulfonyl-N1-acylbenzamidines and N2-arylsulfonyl-N1,N1-diacylbenzamidines.The hydrolysis and ammonolysis of the compounds were studied, and their IR spectra are discussed.It was established that the reactin of arenesulfonamides with the nitriles of aromatic acids in the presence of the alkaline or acidic catalysts leads to the formation of N2-(arylsulfonyl)amidines.

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