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2,2,5-Trimethyl-1-phenyl-3-phenylsulfanyl-hex-5-en-1-one is a complex organic compound characterized by its unique molecular structure. It features a hexenone backbone with a triple bond between the 4th and 5th carbon atoms, which contributes to its reactivity. The molecule is adorned with three methyl groups at the 2nd, 2nd, and 5th carbon positions, enhancing its steric properties. A phenyl group is attached to the 1st carbon, providing aromatic character, while a phenylsulfanyl group is connected to the 3rd carbon, introducing sulfur into the molecule. This combination of functional groups and structural elements gives rise to a variety of chemical properties and potential applications in fields such as pharmaceuticals, fragrances, and materials science.

83180-99-8

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83180-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83180-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,8 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83180-99:
(7*8)+(6*3)+(5*1)+(4*8)+(3*0)+(2*9)+(1*9)=138
138 % 10 = 8
So 83180-99-8 is a valid CAS Registry Number.

83180-99-8Relevant academic research and scientific papers

O-SILYLATED ENOLATE PHENYLTHIOALKYLATION: A NEW SYNTHESIS OF UNSATURATED 1,5-DICARBONYL COMPOUNDS.

Khan, Hassan A.,Paterson, Ian

, p. 2399 - 2402 (2007/10/02)

The O-silylated enolates of ketones and esters can be phenylthioalkylated by the chlorides (2) and (3) under ZnBr2-catalysis; ozonolysis and subsequent sulphoxide thermolysis then gives the corresponding unsaturated 1,5-dicarbonyl compounds.

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