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26824-02-2

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26824-02-2 Usage

General Description

2-Mercaptoacetophenone is a chemical compound that consists of a phenyl ring with a thiol group and a ketone group attached to it. It is commonly used as a fragrance and flavoring agent in the food and cosmetic industry, and as a reagent in organic synthesis. The compound has a strong sulfurous odor and is colorless to pale yellow in appearance. It is also known for its ability to act as a chelating agent, and for its potential applications in pharmaceuticals and agrochemicals. Due to its distinct aroma and chemical properties, 2-mercaptoacetophenone has a wide range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 26824-02-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,8,2 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26824-02:
(7*2)+(6*6)+(5*8)+(4*2)+(3*4)+(2*0)+(1*2)=112
112 % 10 = 2
So 26824-02-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8OS/c9-8(6-10)7-4-2-1-3-5-7/h1-5,10H,6H2

26824-02-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-mercaptoacetophenone

1.2 Other means of identification

Product number -
Other names 2-thioacetophenone

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:26824-02-2 SDS

26824-02-2Relevant articles and documents

Loveridge et al.

, p. 221 (1971)

Substituted Benzothietes: Synthesis and a Quantum Chemical Investigation of Their Cycloreversion Properties

Ahlburg, Nils L.,Velarde, Andres R.,Kieber-Emmons, Matthew T.,Jones, Peter G.,Werz, Daniel B.

supporting information, p. 4255 - 4260 (2020/06/04)

A flexible synthesis for highly substituted benzothietes that does not require flash-vacuum pyrolysis was developed. This allows for the use of a number of functional groups and nonvaporizable molecules. Highly stabilized derivatives were isolated. The molecular orbital properties of various benzothietes were evaluated by density functional methods. The mechanism of the cycloreversion of the four-membered ring was compared to that of the oxygen-containing analogues.

Synthetic quinolone signal analogues inhibiting the virulence factor elastase of Pseudomonas aeruginosa

Szamosvári, Dávid,Reichle, Valentin F.,Jureschi, Monica,B?ttcher, Thomas

supporting information, p. 13440 - 13443 (2016/11/19)

We explore the chemical space of Pseudomonas quinolone signal analogs as privileged structures and report the discovery of a thioquinolone as a potent inhibitor of the important virulence factor elastase of the human pathogen Pseudomonas aeruginosa. We provide evidence that the derivative binds to the active site zinc of elastase and additionally acts as a fluorescent zinc sensor.

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