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2-Cyclohexen-1-one, 3-(methylthio)-, also known as 3-(methylthio)cyclohex-2-en-1-one, is an organic compound characterized by a cyclohexenone ring structure with a methylthio group attached at the 3-position. 2-Cyclohexen-1-one, 3-(methylthio)- is a colorless to pale yellow liquid with a molecular formula of C7H12OS and a molecular weight of 140.24 g/mol. It is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and fragrances due to its unique chemical properties and reactivity. The compound is typically synthesized through various chemical reactions, such as the condensation of cyclohexanone with methyl mercaptan, and is used in the preparation of complex organic molecules that require a cyclohexenone or methylthio functional group.

5682-78-0

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5682-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5682-78-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5682-78:
(6*5)+(5*6)+(4*8)+(3*2)+(2*7)+(1*8)=120
120 % 10 = 0
So 5682-78-0 is a valid CAS Registry Number.

5682-78-0Downstream Products

5682-78-0Relevant academic research and scientific papers

A Method for Mild Photochemical Oxidation; Conversion of Phenacyl Sulfides into Carbonyl Compounds

Vedejs, E.,Perry, D. A.

, p. 573 - 575 (2007/10/02)

Sunlamp irradiation of phenacyl sulfides PhCOCH2SCHRR' affords thiocarbonyl compounds S=CRR' that can be trapped in high yield by using the nitronate CH3CH=N+(OTBS)O-; the heterocycle 3 resulting from 1,3-dipolar cycloaddition is cleaved rapidly by fluoride ion to give ketones or aldehydes.

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