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(3R,6S)-3,6-Diphenyl-3,6-dihydro-thiopyran-2,2-dicarboxylic acid diamide is a complex organic compound with a unique molecular structure. It is characterized by its thiopyran ring, which is a heterocyclic compound containing a sulfur atom in the ring structure. The compound features two phenyl groups attached to the 3 and 6 positions of the thiopyran ring, and a diamide group at the 2,2-dicarboxylic acid positions. This specific arrangement of atoms and functional groups gives the compound its distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science. The chirality of the compound is indicated by the (3R,6S) notation, which describes the spatial arrangement of the phenyl groups around the chiral centers at the 3 and 6 positions.

79562-71-3

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79562-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79562-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,5,6 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79562-71:
(7*7)+(6*9)+(5*5)+(4*6)+(3*2)+(2*7)+(1*1)=173
173 % 10 = 3
So 79562-71-3 is a valid CAS Registry Number.

79562-71-3Relevant academic research and scientific papers

DARSTELLUNG UND DESULFURIERUNG CYCLISCHER α,α-DICYANTHIOALLYLVERBINDUNGEN

Friedrich, Klaus,Gallmeier, Hans-Joachim

, p. 2971 - 2972 (2007/10/02)

Thiomesoxalic acid diamide 1, obtained in situ by reaction of dibromomalonic acid diamide with potassium ethylxantogenate, adds to 1,3-dienes.The cycloadducts 2 upon dehydration yield the dicyanothioethers 3, with are desulfurized with trimethyl phosphite to give the vinylcyclopropane dicarbonitriles 5.

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