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2-[(4-CHLOROBENZYL)SULFANYL]BENZENECARBOXYLIC ACID is a carboxylic acid derivative featuring a benzene ring with a carboxylic acid group and a thioether group. The inclusion of a chlorobenzyl group distinguishes 2-[(4-CHLOROBENZYL)SULFANYL]BENZENECARBOXYLIC ACID as a benzyl chloride derivative. Its structural attributes and functional groups may confer potential applications across various fields, including pharmaceuticals and agrochemicals, and it can also serve as a precursor for synthesizing organic molecules with tailored properties and functions.

15887-84-0

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15887-84-0 Usage

Uses

Used in Pharmaceutical Industry:
2-[(4-CHLOROBENZYL)SULFANYL]BENZENECARBOXYLIC ACID is used as a chemical intermediate for the synthesis of pharmaceutical compounds, leveraging its unique structural features to create molecules with specific biological activities and therapeutic potentials.
Used in Agrochemical Industry:
In the agrochemical sector, 2-[(4-CHLOROBENZYL)SULFANYL]BENZENECARBOXYLIC ACID is utilized as a building block for developing agrochemicals, such as pesticides and herbicides, due to its ability to form stable and effective molecules for crop protection.
Used in Organic Synthesis:
2-[(4-CHLOROBENZYL)SULFANYL]BENZENECARBOXYLIC ACID is employed as a key component in organic synthesis processes, enabling the creation of a variety of organic molecules with specialized properties and functions for use in different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 15887-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,8 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15887-84:
(7*1)+(6*5)+(5*8)+(4*8)+(3*7)+(2*8)+(1*4)=150
150 % 10 = 0
So 15887-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C14H11ClO2S/c15-11-7-5-10(6-8-11)9-18-13-4-2-1-3-12(13)14(16)17/h1-8H,9H2,(H,16,17)/p-1

15887-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-Chlorobenzyl)sulfanyl]benzenecarboxylic acid

1.2 Other means of identification

Product number -
Other names 2-[(4-chlorophenyl)methylsulfanyl]benzoate

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:15887-84-0 SDS

15887-84-0Relevant academic research and scientific papers

Photoisomerization in an analogous set of ruthenium sulfoxide complexes

Porter, Brianne L.,McClure, Beth Anne,Abrams, Eric R.,Engle, James T.,Ziegler, Christopher J.,Rack, Jeffrey J.

experimental part, p. 341 - 346 (2011/11/04)

Complexes of the type [Ru(bpy)2(OSOBnR)](PF6) where bpy is 2,2′-bipyridine and OSOBnR is a 4-substituted benzylsulfinylbenzoate with R = NO2, F, Cl, H, CH3, CF3 and OCH3, have been prepared

Design and synthesis of new 2-substituted-5-(2-benzylthiophenyl)-1,3,4- oxadiazoles as benzodiazepine receptor agonists

Zarghi, Afshin,Faizi, Mehrdad,Shafaghi, Bijan,Ahadian, Avideh,Khojastehpoor, Hamid R.,Zanganeh, Vahideh,Tabatabai, Sayyed A.,Shafiee, Abbas

, p. 3126 - 3129 (2007/10/03)

A series of new 2-substituted-5-(2-benzylthiophenyl)-1,3,4-oxadiazoles was designed and synthesized as anticonvulsant agents. Conformational analysis and superimposition of energy minima conformers of the designed molecules on estazolam, a known benzodiazepine receptor agonist, revealed that the main proposed benzodiazepine pharmacophores were well matched. Electroshock and pentylenetetrazole-induced lethal convulsion tests showed that the introduction of an amino group in position 2 of 1,3,4-oxadiazole ring and a fluoro substituent at para position of benzylthio moiety had the best anticonvulsant activity. It seems this effect is mediated through benzodiazepine receptors mechanism.

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