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α(2'-Carbmethoxy-phenylmercapto)-acetophenon is a complex organic chemical compound with the molecular formula C16H14O3S. It is characterized by a phenyl ring with a carbmethoxy group (ester of carboxylic acid and methanol) at the 2' position and a mercapto group (sulfhydryl group) attached to the α-carbon of an acetophenone moiety. α(2'-Carbmethoxy-phenylmercapto)-acetophenon is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structural features. It serves as an important intermediate in the preparation of certain drugs and can be used in the development of new chemical entities with specific therapeutic or pesticidal properties.

53278-12-9

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53278-12-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53278-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,7 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53278-12:
(7*5)+(6*3)+(5*2)+(4*7)+(3*8)+(2*1)+(1*2)=119
119 % 10 = 9
So 53278-12-9 is a valid CAS Registry Number.

53278-12-9Downstream Products

53278-12-9Relevant academic research and scientific papers

Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold

Rotondi, Giulia,Guglielmi, Paolo,Carradori, Simone,Secci, Daniela,De Monte, Celeste,De Filippis, Barbara,Maccallini, Cristina,Amoroso, Rosa,Cirilli, Roberto,Akdemir, Atilla,Angeli, Andrea,Supuran, Claudiu T.

, p. 1400 - 1413 (2019/08/26)

A large library of derivatives based on the scaffold of 2-(benzylsulfinyl)benzoic acid were synthesised and tested as atypical inhibitors against four different isoforms of human carbonic anhydrase (hCA I, II, IX and XII, EC 4.2.1.1). The exploration of the chemical space around the main functional groups led to the discovery of selective hCA IX inhibitors in the micromolar/nanomolar range, thus establishing robust structure-activity relationships within this versatile scaffold. HPLC separation of some selected chiral compounds and biological evaluation of the corresponding enantiomers was performed along with molecular modelling studies on the most active derivatives.

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