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3724-10-5

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3724-10-5 Usage

Uses

2-(Methylthio)benzoic acid is used as an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dye stuffs.

Check Digit Verification of cas no

The CAS Registry Mumber 3724-10-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,2 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3724-10:
(6*3)+(5*7)+(4*2)+(3*4)+(2*1)+(1*0)=75
75 % 10 = 5
So 3724-10-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O2S/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3,(H,9,10)/p-1

3724-10-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A10379)  2-(Methylthio)benzoic acid, 98+%   

  • 3724-10-5

  • 5g

  • 1056.0CNY

  • Detail
  • Alfa Aesar

  • (A10379)  2-(Methylthio)benzoic acid, 98+%   

  • 3724-10-5

  • 25g

  • 3612.0CNY

  • Detail

3724-10-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(METHYLTHIO)BENZOIC ACID

1.2 Other means of identification

Product number -
Other names 2-(Methylthio)benzoic Acid

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:3724-10-5 SDS

3724-10-5Relevant articles and documents

Rearrangements in the Molecular Ion of o-(Methyl-d3-thio)benzoic acid: Comparison with o-Methoxy-d3-benzoic Acid

Gillis, Richard G.,Porter, Quentin N.

, p. 543 - 545 (1985)

Hydrogen/deuterium exchange and rearrangements in the molecular ion of o-(methyl-d3-thio)benzoic acid lead to fragment ions + as well as + and m/z 106 and 107, just as in the molecular ion of o-methoxybenzoic a

Photocatalytic Deoxygenation of Sulfoxides Using Visible Light: Mechanistic Investigations and Synthetic Applications

Clarke, Aimee K.,Parkin, Alison,Rossi-Ashton, James A.,Taylor, Richard J. K.,Unsworth, William P.

, p. 5814 - 5820 (2020/07/21)

The photocatalytic deoxygenation of sulfoxides to generate sulfides facilitated by either Ir[(dF(CF3)ppy)2(dtbbpy)]PF6 or fac-Ir(ppy)3 is reported. Mechanistic studies indicate that a radical chain mechanism operates, which proceeds via a phosphoranyl radical generated from a radical/polar crossover process. Initiation of the radical chain was found to proceed via two opposing photocatalytic quenching mechanisms, offering complementary reactivity. The mild nature of the radical deoxygenation process enables the reduction of a wide range of functionalized sulfoxides, including those containing acid-sensitive groups, in typically high isolated yields.

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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