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839-48-5

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839-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 839-48-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 839-48:
(5*8)+(4*3)+(3*9)+(2*4)+(1*8)=95
95 % 10 = 5
So 839-48-5 is a valid CAS Registry Number.

839-48-5SDS

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-benzoyl-benzeneiminosulfonyl chloride

1.2 Other means of identification

Product number -
Other names N-benzoyl-benzenesulfonimidoyl chloride

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:839-48-5 SDS

839-48-5Relevant articles and documents

Direct Synthesis of N-Acyl Sulfonimidamides and N-Sulfonimidoyl Amidines from Sulfonimidoyl Azides

Nandi, Ganesh Chandra,Jesin, Irfana

supporting information, p. 2465 - 2469 (2018/05/30)

Herein, we describe the preparation of sulfonimidoyl azides, and demonstrate their utility in the construction of N-acyl sulfonimidamides and N-sulfonimidoyl amidines. N-Acyl sulfonimidamides were synthesized in good to very good yields via “on water” cop

Synthesis of CF3-substituted sulfoximines from sulfonimidoyl fluorides

Kowalczyk, Rafal,Edmunds, Andrew J. F.,Hall, Roger G.,Bolm, Carsten

supporting information; experimental part, p. 768 - 771 (2011/04/24)

N-Protected trifluoromethyl-substituted sulfoximines have been prepared by treatment of sulfonimidoyl fluorides with a combination of the Ruppert-Prakash reagent (TMSCF3) and tetrabutyl ammonium fluoride (TBAF). The starting materials were accessed following two synthetic routes, and for each reaction sequence the substrate scope was evaluated. Accordingly, a wide variety of aryl-substituted products were obtained in moderate to good yield.

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