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(3R,6R)-3,6-Bis-benzylsulfanyl-1,4-dimethyl-piperazine-2,5-dione is a complex organic compound with the molecular formula C21H24N2O2S2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and it is characterized by its specific (3R,6R) configuration. (3R,6R)-3,6-Bis-benzylsulfanyl-1,4-dimethyl-piperazine-2,5-dione features a piperazine-2,5-dione core, which is a cyclic structure with two carbonyl groups at the 2 and 5 positions. The molecule is further functionalized with two benzylsulfanyl groups attached to the 3 and 6 positions of the piperazine ring. Benzylsulfanyl groups are derived from benzyl and sulfanyl moieties, contributing to the compound's unique chemical properties. This specific arrangement of atoms and functional groups gives the compound its distinct chemical and physical characteristics, which may be relevant in various chemical or pharmaceutical applications.

79247-57-7

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79247-57-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79247-57-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,4 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79247-57:
(7*7)+(6*9)+(5*2)+(4*4)+(3*7)+(2*5)+(1*7)=167
167 % 10 = 7
So 79247-57-7 is a valid CAS Registry Number.

79247-57-7Relevant academic research and scientific papers

TOTAL SYNTHESIS OF GLIOTOXIN, DEHYDROGLIOTOXIN AND HYALODENDRIN

Fukuyama, Tohru,Nakatsuka, Shin-Ichi,Kishi, Yoshito

, p. 2045 - 2078 (2007/10/02)

Two general methods, Method A and Method B in Scheme 19, to synthesize epidithiapiperazinediones, are described.A total synthesis of racemic and optically active gliotoxin (1) and of racemic dehydrogliotoxin (53) was achieved by using Method A, whereas a total synthesis of racemic hyalodendrin (52) was completed by using Method B.

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