1668-07-1 Usage
Description
(3R)-2,3-Dihydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-10H-3α,10aα-epidithiopyrazino[1,2-a]indole-1,4-dione is a pyrazinoindole derivative with the molecular formula C15H15NO5S2. It features a 3α,10aα-epidithio substitution pattern and a dihydroxy-substituted indole core, with a hydroxymethyl group linked to the 3-position. The unique chemical structure suggests potential reactivity and pharmacological properties, making it a promising candidate for synthetic and medicinal chemistry research.
Uses
Used in Pharmaceutical Industry:
(3R)-2,3-Dihydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-10H-3α,10aα-epidithiopyrazino[1,2-a]indole-1,4-dione is used as a pharmaceutical compound for its potential biological activity. (3R)-2,3-Dihydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-10H-3α,10aα-epidithiopyrazino[1,2-a]indole-1,4-dione's unique structure and functional groups may contribute to its interaction with biological targets, offering opportunities for the development of new drugs and therapies.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (3R)-2,3-Dihydro-6-hydroxy-3-(hydroxymethyl)-2-methyl-10H-3α,10aα-epidithiopyrazino[1,2-a]indole-1,4-dione serves as a valuable target for synthetic studies. Its chemical properties and potential reactivity make it an interesting subject for exploring novel synthetic pathways and developing new chemical entities with potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1668-07-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1668-07:
(6*1)+(5*6)+(4*6)+(3*8)+(2*0)+(1*7)=91
91 % 10 = 1
So 1668-07-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O4S2/c1-14-10(18)12-5-7-3-2-4-8(17)9(7)15(12)11(19)13(14,6-16)21-20-12/h2-4,16-17H,5-6H2,1H3/t12?,13-/m1/s1
1668-07-1Relevant articles and documents
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Herrmann,H. et al.
, p. 4315 - 4319 (1964)
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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.
