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130552-90-8

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130552-90-8 Usage

General Description

(E)-N-benzylidenebenzenesulfonamide is a chemical compound that is also known as benzenesulfonamide or benzenesulfonyl benzylideneamine. (E)-N-benzylidenebenzenesulfonamide is a sulfonamide derivative and has the molecular formula C13H11NO2S. It is commonly used as a building block in the synthesis of various organic compounds and pharmaceuticals. (E)-N-benzylidenebenzenesulfonamide has been studied for its potential biological activities, including anti-cancer and anti-inflammatory properties. It is also known for its ability to form coordination complexes with various metal ions, making it useful in catalysis and materials science. However, it should be handled with caution as it can be harmful if ingested or comes into contact with the skin or eyes.

Check Digit Verification of cas no

The CAS Registry Mumber 130552-90-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,5 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 130552-90:
(8*1)+(7*3)+(6*0)+(5*5)+(4*5)+(3*2)+(2*9)+(1*0)=98
98 % 10 = 8
So 130552-90-8 is a valid CAS Registry Number.

130552-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(E)-Phenylmethylene]benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-benzyl-but-2-enamide

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:130552-90-8 SDS

130552-90-8Relevant articles and documents

Synthesis of 2-chloro-2-imidoylaziridines via aza-darzens-type reaction of 3,3-dichloro-1-azaallylic anions and N-(arylsulfonyl)imines

Giubellina, Nicola,Mangelinckx, Sven,Toernroos, Karl W.,De Kimpe, Norbert

, p. 5881 - 5887 (2007/10/03)

3,3-Dichloro-1-azaallylic anions, generated by deprotonation of α,α-dichloroketimines 10 with lithium diisopropylamide, reacted with N-sulfonylaldimines 7 to produce the Mannich-type products N-[2,2-dichloro-3- (N-alkylimino)-1,3-diarylpropyl]benzenesulfo

An easy synthesis of aliphatic and aromatic N-sulfonyl aldimines

Chemla, Fabrice,Hebbe, Virginie,Normant, Jean-F.

, p. 75 - 77 (2007/10/03)

N-Arenesulfonyl aldimines were prepared from aliphatic and aromatic aldehydes in a two-step transformation.

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