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Benzenesulfonimidoyl chloride, N-benzoyl-, also known as N-benzoylbenzenesulfonimidoyl chloride, is an organic compound with the chemical formula C13H10ClNO2S. It is a white crystalline solid that is soluble in organic solvents such as dichloromethane and acetonitrile. Benzenesulfonimidoyl chloride, N-benzoyl- is primarily used as a reagent in organic synthesis, particularly in the preparation of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is known for its ability to act as a protecting group in peptide synthesis and as a coupling agent in the formation of amide bonds. Due to its reactivity, it is essential to handle Benzenesulfonimidoyl chloride, N-benzoyl- with care, typically under an inert atmosphere and at low temperatures to prevent unwanted side reactions.

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 academic research and scientific papers

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 and arylation of unprotected sulfonimidamides

Funes Maldonado, Matías,Sehgelmeble, Fernando,Bjarnemark, Fanny,Svensson, Mats,?hman, Jens,Arvidsson, Per I.

, p. 7456 - 7462 (2012/09/22)

Herein we evaluate different methodologies for the synthesis of unprotected sulfonimidamides. Three different procedures that allow orthogonal deprotection of the imine nitrogen under acidic, nucleophilic, and basic conditions were established. Moreover,

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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