67532-32-5 Usage
Chemical Family
2(3H)-Furanone, dihydro-5-phenyl-4-(phenylthio)belongs to the furanone family.
Derivative
It is a dihydro derivative of 5-phenyl-4-(phenylthio)furan-2(3H)-one.
Physical State
2(3H)-Furanone, dihydro-5-phenyl-4-(phenylthio)is a colorless liquid.
Molecular Weight
Its molecular weight is 254.34 g/mol.
Usage
It is commonly used in organic synthesis and pharmaceutical research due to its unique aromatic and sulfur-containing properties.
Potential Applications
Its potential applications include as a fragrance in perfumes and as an intermediate in the synthesis of biologically active compounds.
Pharmacological Activities
2(3H)-Furanone, dihydro-5-phenyl-4-(phenylthio)has been studied for its potential pharmacological activities, such as its antimicrobial and antioxidative properties.
Check Digit Verification of cas no
The CAS Registry Mumber 67532-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,3 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67532-32:
(7*6)+(6*7)+(5*5)+(4*3)+(3*2)+(2*3)+(1*2)=135
135 % 10 = 5
So 67532-32-5 is a valid CAS Registry Number.
67532-32-5Relevant articles and documents
Iron-Catalyzed Radical Annulation of Unsaturated Carboxylic Acids with Disulfides for the Synthesis of γ-Lactones
Cheng, Fei,Wang, Li-Li,Mao, Yuan-Hu,Dong, Yong-Xi,Liu, Bin,Zhu, Gao-Feng,Yang, Yuan-Yong,Guo, Bing,Tang, Lei,Zhang, Ji-Quan
, p. 8620 - 8629 (2021)
An efficient aerobic iron-catalyzed annulation of unsaturated carboxylic acids with disulfides has been developed. This procedure proceeds using FeCl3as the catalyst and KI as an iodine source under an air atmosphere, which provides practical access to a wide range of substituted γ-lactone derivatives. The disclosed method is quite simple, highly atom-economic, environmentally friendly, and tolerates a broad substrate scope.
EXTENDED ENOLATE IONS FROM γ-PHENYLTHIO-CROTONATE ESTERS
Brownbridge, Peter,Hunt, Paul G.,Warren, Stuart
, p. 3391 - 3394 (2007/10/02)
Substituted γ-phenylthio-crotonate esters (7) can be made by and PhS shifts: they form extended enolate anions which react with electrophiles at the carbon atom α to the carbonyl group and γ to sulphur.
