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N-benzyl-N-phenylbenzenesulfonamide is an organic compound with the chemical formula C19H18NO2S. It is a derivative of benzenesulfonamide, featuring a benzyl group attached to the nitrogen atom, and a phenyl group attached to the other nitrogen atom. N-benzyl-N-phenylbenzenesulfonamide is characterized by its white crystalline appearance and is soluble in organic solvents such as ethanol and acetone. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. Due to its unique structure, it exhibits specific chemical properties, making it a valuable building block in the development of new compounds with potential applications in various industries.

1096-43-1

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1096-43-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1096-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 6 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1096-43:
(6*1)+(5*0)+(4*9)+(3*6)+(2*4)+(1*3)=71
71 % 10 = 1
So 1096-43-1 is a valid CAS Registry Number.

1096-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-benzenesulfonylanilide

1.2 Other means of identification

Product number -
Other names N-Benzyl-N-phenyl-p-benzolsulfonamid

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:1096-43-1 SDS

1096-43-1Downstream Products

1096-43-1Relevant academic research and scientific papers

Mechanistic insight into thermal 1,3- and 1,5-sulfonyl migrations of N-arenesulfonylphenothiazines and N-arenesulfonylphenoxazines

Wang, Jiandong,Son, Kwon-Il,Xu, Jiaxi

, p. 1637 - 1649 (2016/08/16)

The substrate scope and mechanistic insight of the thermal-induced 1,3- and 1,5-sulfonyl migration reactions of various sulfonamides have been investigated. The results indicate that both N-arenesulfonylphenothiazines and N-arenesulfonylphenoxazines can u

Solvent free N-alkylation of phenyl sulfanilides under microwave irradiation

Jaisankar,Srinivasan

, p. 1048 - 1050 (2007/10/03)

A facile N-alkylation of phenylsulfanilides by reaction with primary alkyl halides (benzyl bromide, ethyl bromoacetate and n-butyl bromide) in the presence of anhydrous potassium carbonate under microwave condition to give N-alkylated products in good yields is reported.

Heterocycles in Organic Synthesis. Part 42. Preparation of Azides, Phthalimides, and Sulphonamides from Primary Amines

Katritzky, Alan R.,Liso, Gaietano,Lunt, Edward,Patel, Ranjan C.,Thind, Sukhpal S.,Zia, Abid

, p. 849 - 851 (2007/10/02)

N-Alkyl and N-benzyl substituents are displaced from 2,4,6-triphenylpyridinium cations by nucleophilic azide, phthalimide, succinimide, and sulphonamide anions.This enables the conversion of primary alkyl- and benzylamines into azides, and primary (with potential for inversion or labelling) and secondary amines.

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