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Benzamide, N-[N-benzoyl-S-(4-chlorophenyl)sulfinimidoyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81386-74-5

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81386-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81386-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,8 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81386-74:
(7*8)+(6*1)+(5*3)+(4*8)+(3*6)+(2*7)+(1*4)=145
145 % 10 = 5
So 81386-74-5 is a valid CAS Registry Number.

81386-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[N-benzoyl-S-(4-chlorophenyl)sulfinimidoyl]benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-[N-benzoyl-S-(4-chlorophenyl)sulfinimidoyl]

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:81386-74-5 SDS

81386-74-5Relevant academic research and scientific papers

REACTION OF DIARYL DISULFIDES WITH N-CHLOROAMIDES OF CARBOXYLIC ACIDS

Levchenko, E. S.,Dubinina, T. N.,Budnik, L. V.

, p. 1875 - 1880 (2007/10/02)

In the reaction of diaryl disulfides with N-chlorocarboxamides arenesulfenyl chlorides and N-acylarenesulfenamides are formed initially.The subsequent reaction path is determined by the reaction of the latter with the N-chlorocarboxamides, and N-acylarenesulfinimidoyl chlorides, N,N'-diacylaryldiazasulfonium chlorides, or N,N'-diacylarenesulfinamidines are formed, depending on the ratio of the reagents and on the reaction conditions.

OXIDATION IMINATION OF SULFENYL CHLORIDES BY N-CHLOROCARBOXAMIDES. N-ACYLSULFINIMIDOYL CHLORIDES

Dubinina, T. N.,Levchenko, E. S.,Zabolotnaya, T. G.

, p. 143 - 148 (2007/10/02)

The reaction of arenesulfenyl chlorides ArSCl with N-chlorocarboxyamides in a ratio of 1:1 leads to the formation of N-acylsulfinimidoyl chlorides ArS(=NCOR)Cl.The reaction of arenesulfenyl chlorides and N-chlorobenzamide in ratio of 1:1 leads to aryldibenzamidosulfonium chlorides ArS(NHCOC6H5)2, which are hydrolyzed with the formation of N,N'-benzoylarenesulfinamidines ArS(=NCOC6H5)NHCOC6H5 and are cleaved into acid chlorides and benzamide when heated.

CHEMISTRY OF IMINOSULFINIC ACIDS. REACTION OF N-ACYLIMINOSULFINYL CHLORIDES WITH THIOPHENOLS

Levchenko, E. S.,Pel'kis, N. P.,Kalinin, V. N.,Duzhak, A. A.

, p. 1028 - 1033 (2007/10/02)

Arene(N-benzoyl)- and arene(N-phenylsulfonyl)iminosulfinyl chlorides on reaction with thiophenols are reduced to N-(benzoyl) or N-(phenylsulfonyl)arenesulfenamides.When N-benzoyliminosulfinyl chlorides are reacted with thiophenols in the presence of triethylamine, a mixture of diaryl sulfides, NN-di(arylthio)benzamide, and N-arylthio-NN'-dibenzoylarenesulfinamidines is obtained.On heating, the latter reversibly dissociate to stable N-arylthio-N-benzoylaminyl radicals.

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