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The chemical compound "(1RS)-6-((1SR)-6t-acetoxy-2-chloromethyl-cyclohexa-2,4-dien-r-yl)-3ξ-(4-methoxy-phenyl)-8-methyl-2,4-dithia-6,8-diaza-bicyclo[3.2.2]nonane-7,9-dione" is a complex organic molecule with a unique structure. It features a bicyclo[3.2.2]nonane core, which is a nine-membered ring system with two nitrogen atoms and two sulfur atoms incorporated into the ring, forming a 2,4-dithia-6,8-diaza structure. The molecule also includes a cyclohexa-2,4-dien-1-yl group with a 6t-acetoxy-2-chloromethyl substitution, indicating the presence of an acetoxy group and a chloromethyl group at specific positions. Additionally, a 4-methoxy-phenyl group is attached to the molecule, contributing to its overall structure and potential reactivity. (1RS)-6-((1SR)-6t-acetoxy-2-chloromethyl-cyclohexa-2,4-dien-r-yl)-3ξ-(4-methoxy-phenyl)-8-methyl-2,4-dithia-6,8-diaza-bicyclo[3.2.2]nonane-7,9-dione is characterized by its intricate arrangement of atoms and functional groups, which may have implications for its chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

79355-33-2

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79355-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79355-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,5 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79355-33:
(7*7)+(6*9)+(5*3)+(4*5)+(3*5)+(2*3)+(1*3)=162
162 % 10 = 2
So 79355-33-2 is a valid CAS Registry Number.

79355-33-2Upstream product

79355-33-2Relevant 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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