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2,2,5,5-Tetraphenyl-[1,3]dithiolane-4-carboxylic acid methyl ester is a complex organic compound characterized by its unique molecular structure. It features a [1,3]dithiolane ring, which is a five-membered ring containing two sulfur atoms, and is adorned with four phenyl groups, each consisting of a benzene ring. The carboxylic acid group is located at the 4-position of the dithiolane ring, and it is esterified with a methyl group, making it a methyl ester. 2,2,5,5-Tetraphenyl-[1,3]dithiolane-4-carboxylic acid methyl ester is known for its potential applications in the synthesis of various organic compounds and materials, particularly in the field of pharmaceuticals and specialty chemicals. Its chemical properties and reactivity make it a valuable intermediate in the preparation of certain drugs and other chemical products.

81113-45-3

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81113-45-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81113-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,1 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81113-45:
(7*8)+(6*1)+(5*1)+(4*1)+(3*3)+(2*4)+(1*5)=93
93 % 10 = 3
So 81113-45-3 is a valid CAS Registry Number.

81113-45-3Relevant academic research and scientific papers

THE REACTION OF DIAZOACETIC ESTER WITH THIOBENZOPHENONE

Kalwinsch, Ivars,Huisgen, Rolf

, p. 3941 - 3944 (2007/10/02)

Methyl diazoacetate reacts with two equivalents of thiobenzophenone to furnish two isomeric 1,3-dithiolanes and nitrogen; the intermediate thiocarbonyl ylide is intercepted by 1,3-dipolar cycloaddition or undergoes electrocyclic ring closure.

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