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17839-61-1

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17839-61-1 Usage

General Description

2-(butylthio)benzoic acid is an organic compound with the chemical formula C11H14O2S. It is a derivative of benzoic acid, containing a butylthio group attached to the benzene ring. 2-(butylthio)benzoic acid is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. It has potential applications in the development of anti-inflammatory, anti-fungal, and anti-bacterial agents due to its structural characteristics and properties. Additionally, 2-(butylthio)benzoic acid may also be used as a reagent in organic chemistry reactions for the creation of new compounds with desired properties.

Check Digit Verification of cas no

The CAS Registry Mumber 17839-61-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,3 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17839-61:
(7*1)+(6*7)+(5*8)+(4*3)+(3*9)+(2*6)+(1*1)=141
141 % 10 = 1
So 17839-61-1 is a valid CAS Registry Number.

17839-61-1Relevant articles and documents

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.

Cytotoxicity of copper(II)-complexes with some S-alkyl derivatives of thiosalicylic acid. Crystal structure of the binuclear copper(II)-complex with S-ethyl derivative of thiosalicylic acid

Nikoli?, Milo? V.,Mijajlovi?, Marina ?.,Jevti?, Verica V.,Ratkovi?, Zoran R.,Novakovi?, Sladjana B.,Bogdanovi?, Goran A.,Milovanovi?, Jelena,Arsenijevi?, Aleksandar,Stojanovi?, Bojana,Trifunovi?, Sre?ko R.,Radi?, Gordana P.

, p. 264 - 271 (2016/04/04)

The spectroscopically predicted structure of the obtained copper(II)-complex with S-ethyl derivative of thiosalicylic acid was confirmed by X-ray structural study and compared to previously reported crystal structure of the Cu complex with S-methyl deriva

Cytotoxicity of palladium(II) complexes with some alkyl derivates of thiosalicylic acid. Crystal structure of the bis(S-butyl-thiosalicylate)palladium(II) complex, [Pd(S-bu-thiosal)2]

Mijajlovi?, Marina ?.,Nikoli?, Milo? V.,Jevti?, Verica V.,Ratkovi?, Zoran R.,Markovi?, Bojana Simovi?,Volarevi?, Vladislav,Arsenijevi?, Neboj?a N.,Novakovi?, Sladjana B.,Bogdanovi?, Goran A.,Trifunovi?, Sre?ko R.,Radi?, Gordana P.

, p. 34 - 40 (2015/03/04)

The spectroscopically predicted structure of the obtained bis(S-butyl-thiosalicylate)palladium(II) complex, [Pd(S-bu-thiosal)2], was confirmed by an X-ray structural study. The asymmetric unit of [Pd(S-bu-thiosal)2] consists of neutr

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