130552-90-8 Usage
Description
(E)-N-benzylidenebenzenesulfonamide, also known as benzenesulfonamide or benzenesulfonyl benzylideneamine, is a chemical compound belonging to the sulfonamide class. It has the molecular formula C13H11NO2S and is recognized for its potential applications in various fields due to its unique chemical properties.
Uses
Used in Pharmaceutical Synthesis:
(E)-N-benzylidenebenzenesulfonamide is used as a building block for the synthesis of various organic compounds and pharmaceuticals. Its unique structure allows it to be a valuable component in the development of new drugs and medications.
Used in Biological Research:
(E)-N-benzylidenebenzenesulfonamide is used as a subject of study for its potential biological activities, such as anti-cancer and anti-inflammatory properties. Researchers are interested in understanding how this compound interacts with biological systems and how it can be utilized for therapeutic purposes.
Used in Coordination Chemistry:
(E)-N-benzylidenebenzenesulfonamide is used in the formation of coordination complexes with various metal ions. This property makes it a useful compound in the field of catalysis and materials science, where it can contribute to the development of new catalysts and materials with specific properties.
Safety Precautions:
It is important to handle (E)-N-benzylidenebenzenesulfonamide with caution, as it can be harmful if ingested or if it comes into contact with the skin or eyes. Proper safety measures should be taken during its use and storage to minimize the risk of exposure.
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.
130552-90-8Relevant 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.
