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Beta-thionaphthyl acetate, also known as 2-(acetylthio)naphthalene, is an organic compound with the chemical formula C12H10OS. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents. BETA-THIONAPHTHYL ACETATE is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Beta-thionaphthyl acetate is known for its reactivity and can undergo various chemical transformations, making it a valuable building block in the creation of complex molecules. It is also used in the preparation of dyes and pigments, as well as in the production of certain types of plastics and resins. Due to its potential applications and reactivity, beta-thionaphthyl acetate is an important compound in the field of organic chemistry.

831-23-2

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831-23-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 831-23-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 831-23:
(5*8)+(4*3)+(3*1)+(2*2)+(1*3)=62
62 % 10 = 2
So 831-23-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H10OS/c1-9(13)14-12-7-6-10-4-2-3-5-11(10)8-12/h2-8H,1H3

831-23-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name S-naphthalen-2-yl ethanethioate

1.2 Other means of identification

Product number -
Other names |A-Thionaphthyl acetate

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:831-23-2 SDS

831-23-2Relevant academic research and scientific papers

THE REACTIVITY OF SULFUR NUCLEOPHILES TOWARDS ARENEDIAZONIUM TETRAFLUOROBORATES IN APROTIC SOLVENTS: SYNTHESIS OF S-ARYL THIOACETATES

Petrillo, Giovanni,Novi, Marino,Garbarino, Giacomo,Filiberti, Marcos

, p. 4185 - 4188 (2007/10/02)

Various S-aryl thioacetates are prepared in 40-60percent yield by treatment of arenediazonium tetrafluoroborates with commercial potassium thioacetate in DMSO at room temperature.

Modified Molybdenum Carbonyl Species; Excellent Reagents for the Desulphurization of Thiols

Alper, Howard,Blais, Claude

, p. 169 - 170 (2007/10/02)

Thiols can be desulfurized in good yields by treatment with molybdenum hexacarbonyl either in acetic acid or when pre-adsorbed on to silica.

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