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2-[(2-hydroxyethyl)sulfanyl]benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58980-52-2

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58980-52-2 Usage

Molar mass

202.24 g/mol

Physical form

White crystalline solid

Uses

Synthesis of various pharmaceuticals, potential intermediate in the production of other organic compounds, and may have applications in medicinal chemistry and drug development.

Potential

Can be used as a starting material for the synthesis of various derivatives with different properties and functions for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 58980-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,8 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58980-52:
(7*5)+(6*8)+(5*9)+(4*8)+(3*0)+(2*5)+(1*2)=172
172 % 10 = 2
So 58980-52-2 is a valid CAS Registry Number.

58980-52-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-hydroxyethylsulfanyl)benzoic acid

1.2 Other means of identification

Product number -
Other names -

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:58980-52-2 SDS

58980-52-2Relevant academic research and scientific papers

Cu-Mediated C-H Thioetherification of Arenes at Room Temperature

Wang, Xing,Yi, Xing,Xu, Hui,Dai, Hui-Xiong

supporting information, p. 5981 - 5985 (2019/08/26)

Cu-mediated C-H thioetherification of arenes with ethylene sulfide has been developed using a readily removable directing group. The reaction proceeded at room temperature, and a variety of sensitive functional groups including chloro, bromo, and vinyl were well tolerated. The thiolated products could be converted to the seven-membered benzoxathiepinones derivatives by a sequence of hydrolysis-lactonization reactions.

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