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3-phenyl-3-(p-tolylthio)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

412339-56-1

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412339-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 412339-56-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,2,3,3 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 412339-56:
(8*4)+(7*1)+(6*2)+(5*3)+(4*3)+(3*9)+(2*5)+(1*6)=121
121 % 10 = 1
So 412339-56-1 is a valid CAS Registry Number.

412339-56-1SDS

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 3-phenyl-3-p-tolylsulfanyl-propionic acid

1.2 Other means of identification

Product number -
Other names β-p-Tolylmercapto-hydrozimtsaeure

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:412339-56-1 SDS

412339-56-1Relevant academic research and scientific papers

Visible-Light-Driven Iron-Promoted Thiocarboxylation of Styrenes and Acrylates with CO2

Ye, Jian-Heng,Miao, Meng,Huang, He,Yan, Si-Shun,Yin, Zhu-Bao,Zhou, Wen-Jun,Yu, Da-Gang

supporting information, p. 15416 - 15420 (2017/11/01)

The first thiocarboxylation of styrenes and acrylates with CO2 was realized by using visible light as a driving force and catalytic iron salts as promoters. A variety of important β-thioacids were obtained in high yields. This multicomponent reaction proceeds in an atom- and redox-economical manner with broad substrate scope under mild reaction conditions. Notably, high regio-, chemo-, and diasteroselectivity are observed. Mechanistic studies indicate that a radical pathway can account for the unusual regioselectivity.

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