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The chemical compound "(1RS)-6-((1SR)-2-chloromethyl-6t-hydroxy-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. The molecule contains a 2,4-dithia-6,8-diaza group, indicating the presence of two sulfur atoms and two nitrogen atoms in the ring. It also has a 4-methoxy-phenyl group attached to the 3ξ position, which introduces a methoxy substituent on the phenyl ring. Additionally, the compound includes a 2-chloromethyl-6t-hydroxy-cyclohexa-2,4-dien-r-yl group at the 6 position, which contributes a chlorine atom and a hydroxyl group to the molecule. The compound's stereochemistry is indicated by the (1RS) and (1SR) prefixes, suggesting the presence of chiral centers. Overall, (1RS)-6-((1SR)-2-chloromethyl-6t-hydroxy-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 structure, which includes elements such as chlorine, sulfur, nitrogen, oxygen, and carbon, arranged in a specific geometric configuration.

61378-00-5

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61378-00-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61378-00-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,7 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61378-00:
(7*6)+(6*1)+(5*3)+(4*7)+(3*8)+(2*0)+(1*0)=115
115 % 10 = 5
So 61378-00-5 is a valid CAS Registry Number.

61378-00-5Upstream product

61378-00-5Relevant 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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