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2-PYRIDYLETHYL THIOLACETATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59020-97-2

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59020-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59020-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,2 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59020-97:
(7*5)+(6*9)+(5*0)+(4*2)+(3*0)+(2*9)+(1*7)=122
122 % 10 = 2
So 59020-97-2 is a valid CAS Registry Number.

59020-97-2SDS

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-Pyridylethyl Thiolacetate

1.2 Other means of identification

Product number -
Other names S-(2-pyridin-2-ylethyl) ethanethioate

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:59020-97-2 SDS

59020-97-2Relevant academic research and scientific papers

PROCESS FOR PREPARING BISPHENOL

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Page/Page column 34, (2011/12/12)

Provided is a process for producing a bisphenol compound stably at a high conversion and with high selectivity over a long period. A process for producing a bisphenol compound by feeding a phenol compound and a carbonyl compound continuously to a reactor packed with an acid catalyst, characterized in that the acid catalyst is a sulfonic-acid-form cation-exchange resin in which part of the sulfo groups have been modified with at least any one of 2-pyridylalkanethiol compounds and 3-pyridylalkanethiol compounds.

Intramolecular assistance of electron transfer from heteroatom compounds. Electrochemical oxidation of 2-(2-pyridyl)ethyl-substituted ethers, sulfides, and selenides

Watanabe, Mitsuru,Suga, Seiji,Yoshida, Jun-Ichi

, p. 243 - 247 (2007/10/03)

Organoheteroatom compounds having a 2-(2-pyridyl)ethyl group were synthesized and their oxidation potentials were determined by rotating disk electrode voltammetry. The oxidation potentials were found to be less positive than those of the corresponding compounds having a phenyl group in place of the pyridyl group. The dynamic coordination of the pyridyl group to the heteroatom, which stabilizes the cation radical intermediate, seems to be responsible for facilitating the electron transfer. The magnitude of the intramolecular assistance increases along with an increase in the oxidation potential of the parent compounds. This tendency can be explained in terms of the energy match between the nonbonding p orbital of the pyridyl nitrogen and the HOMO of the parent heteroatom compound.

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