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5331-38-4

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  • Acetic acid,2-[(2-cyanoethyl)thio]-, ethyl ester

    Cas No: 5331-38-4

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5331-38-4 Usage

General Description

Ethyl [(2-cyanoethyl)sulfanyl]acetate is a chemical compound with the molecular formula C6H9NO2S. It is a clear, colorless liquid with a fruity odor. ethyl [(2-cyanoethyl)sulfanyl]acetate is commonly used as an intermediate in the production of pharmaceuticals, agrochemicals, and organic synthesis. It is also utilized as a solvent in some industrial processes. Ethyl [(2-cyanoethyl)sulfanyl]acetate can undergo various chemical reactions, such as esterification, hydrolysis, and oxidation, which allows it to be used in a wide range of applications. However, it is important to handle this compound with care as it can be irritating to the skin, eyes, and respiratory system.

Check Digit Verification of cas no

The CAS Registry Mumber 5331-38-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5331-38:
(6*5)+(5*3)+(4*3)+(3*1)+(2*3)+(1*8)=74
74 % 10 = 4
So 5331-38-4 is a valid CAS Registry Number.

5331-38-4Downstream Products

5331-38-4Relevant articles and documents

Allylsulfone compound, method of manufacturing allylsulfone compound, and electrolytic solution for electrochemical device

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Paragraph 0053, (2018/11/22)

PROBLEM TO BE SOLVED: To provide a new sulfone compound useful for an aprotic polar solvent, which is excellent in thermal stability with a relatively low melting point, and has low solubility of water and high decomposition voltage characteristics, and also to provide a method for producing the sulfone compound, and an electrolyte for an electrochemical device which is produced using the sulfone compound.SOLUTION: The sulfone compound is represented by formula (1), wherein R represents 1C-6C alkyl.

Synthesis of Alkenyl Sulphoxides by Intramolecular and Intermolecular Addition of Sulphenic Acids to Alkynes

Bell, Richard,Cottam, Peter D.,Davies, John,Jones, D. Neville

, p. 2106 - 2115 (2007/10/02)

Alkyne-ω-sulphenic acids formed by thermolysis of ω-(t-butylsulphinyl)alkynes at 40 deg C cyclized regiospecifically to 2-methylenethiacycloalkane 1-oxides; 2-methylenethietan 1-oxide was not formed in this way. 2-Methylpropane-2-sulphenic acid, obtained by heating di-t-butyl sulphoxide, added regioselectively to oct-1-yne to give predominantly 2-t-butylsulphinyloct-1-ene, which itself decomposed thermally to a mixture of dioctenyl sulphoxides by way of alkenesulphenic acid-dialkyl sulphine interconversions.Benzenesulphenic acid, methanesulphenic acid, and ethoxycarbonylmethanesulphenic acid, conveniently generated by thermolysis of 1-cyano-2-alkyl(or aryl)sulphinylethanes, underwent intermolecular addition to unactivated and activated alkynes regioselectively to give alkenyl sulphoxides in good yields.

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