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Acetic acid, (2-pyridinylthio)-, ethyl ester (9CI), also known as ethyl 2-pyridinethioacetate, is a colorless liquid chemical compound with a strong, unpleasant odor. It is commonly used as a synthetic intermediate in organic chemistry and serves as a building block for the synthesis of various pharmaceuticals and agrochemicals. Due to its flammable and toxic nature, it requires careful handling during its applications in chemical reactions and industrial processes.

28856-92-0

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28856-92-0 Usage

Uses

Used in Organic Synthesis:
Acetic acid, (2-pyridinylthio)-, ethyl ester (9CI) is used as a synthetic intermediate for the production of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a versatile reagent in the synthesis of other compounds, contributing to the development of new and innovative products in the chemical industry.
Used in Chemical Reactions:
As a reagent, acetic acid, (2-pyridinylthio)-, ethyl ester (9CI) is employed in various chemical reactions to facilitate the formation of desired products. Its reactivity and functional groups make it a valuable component in the synthesis of complex organic molecules, enhancing the efficiency and selectivity of these reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, acetic acid, (2-pyridinylthio)-, ethyl ester (9CI) is used as a key building block for the synthesis of various drugs. Its unique properties enable the development of new therapeutic agents with improved efficacy and reduced side effects, contributing to advancements in medicine and healthcare.
Used in Agrochemical Industry:
Acetic acid, (2-pyridinylthio)-, ethyl ester (9CI) also finds applications in the agrochemical industry, where it is used in the synthesis of various agrochemicals such as pesticides and herbicides. Its role in the development of these products helps improve agricultural productivity and crop protection, ensuring food security and sustainable agriculture practices.

Check Digit Verification of cas no

The CAS Registry Mumber 28856-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,8,5 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28856-92:
(7*2)+(6*8)+(5*8)+(4*5)+(3*6)+(2*9)+(1*2)=160
160 % 10 = 0
So 28856-92-0 is a valid CAS Registry Number.

28856-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-pyridin-2-ylsulfanylacetate

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:28856-92-0 SDS

28856-92-0Relevant articles and documents

Studies on ambiphilic radicals generated from the ester of N-hydroxy-2-thiopyridone

Borah,Sarma

, p. 592 - 596 (2007/10/03)

Seven different α-carbethoxyalkyl radicals have been generated from Barton esters and their behaviour towards different olefins have been studied to show their philicity.

Rate Constants for Chalcogen Group Transfers in Bimolecular Substitution Reactions with Primary Alkyl Radicals

Curran, Dennis P.,Martin-Esker, Amanda A.,Ko, Sung-Bo,Newcomb, Martin

, p. 4691 - 4695 (2007/10/02)

Rate constants for group transfers of the MeS, PhS, PhSe, and PhTe groups from chalcogen-substituted acetate, acetonitrile, malonate, and malononitrile compounds, from N-(phenylthio)phthalimide and from Me2S2 and Ph2S2 to primary alkyl radicals, have been determined by competition kinetics using PTOC esters as the radical precursors and competing trapping agents.Thio group transfers from malononitrile derivatives are marginally faster than the corresponding group transfer from the symmetrical disulfide, and the rate constant for PhSe group transfer from PhSeSePh isgreater than those from the derivatives studied here.Substituent effects suggest that the chalcogen transfer reactions may be concerted.For three cases in which direct comparisons can be made, the rate constants for reactions of phenylchalcogenides are approximately equal to those for halogen atom transfer when the chalcogen and halide are in the same row of the periodic table and the radical resulting from displacement is the same.The rate constants reported in this work will be useful for the rational design of synthetic schemes based on homolytic group transfer chemistry.

Rate Constants for Halogen Atom Transfer from Representative α-Halocarbonyl Compounds to Primary Alkyl Radicals

Curran, Dennis P.,Bosch, Eric,Kaplan, Jere,Newcomb, Martin

, p. 1826 - 1831 (2007/10/02)

Rate constants for halogen atom transfer from diethyl methyliodomalonate (7a), iodoacetonitrile (7b), ethyl 2-methyl-2-iodopropanoate (7c), ethyl iodoacetate (7d), diethyl methylbromomalonate (7e), and ethyl bromoacetate (7f) to simple primary alkyl radicals have been studied by a variety of competition reactions.The Arrhenius functions for halogen atom transfer to the undecyl radical from halides 7d and 7f are log (kI, M-1 s-1) = 10.4 - 4.4/θ and log (kBr, M-1 s-1) = 10.4 - 8.2/θ, respectively.The rate constants for halogen atom transfer to a primaryradical from the series of compounds 7a-7f at 50 deg C are 1.8 x 109, 1.7 x 109, ca. 6 x 108, 2.6 x 107, 1.0 x 106, and 7.0 x 104 M-1 s-1, respectively.The kinetic values are useful for the planning of synthetic methods that incorporate an atom transfer-cyclization process.

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