103470-60-6 Usage
Description
(3R,4S,5S,6S)-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octane-5,6-diol is a complex organic molecule with a unique spirocyclic structure. It features two epoxide (oxiran) rings, one of which is attached to a methyl group and a double bond. (3R,4S,5S,6S)-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octane-5,6-diol also consists of a spirocyclic ring system and two hydroxyl groups. Its stereochemistry is specified by the R and S configurations at different carbon atoms.
Uses
Used in Organic Synthesis:
(3R,4S,5S,6S)-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octane-5,6-diol is used as a key intermediate in organic synthesis for the development of novel compounds with potential applications in various fields.
Used in Medicinal Chemistry:
(3R,4S,5S,6S)-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octane-5,6-diol is used as a building block in the design and synthesis of new pharmaceutical agents, leveraging its unique structure and functional groups to create molecules with potential therapeutic properties.
Used in Biochemical Research:
(3R,4S,5S,6S)-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octane-5,6-diol is used as a research tool in biochemical studies to investigate its interactions with biological systems and explore its potential as a probe for understanding complex biological processes.
Check Digit Verification of cas no
The CAS Registry Mumber 103470-60-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,7 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103470-60:
(8*1)+(7*0)+(6*3)+(5*4)+(4*7)+(3*0)+(2*6)+(1*0)=86
86 % 10 = 6
So 103470-60-6 is a valid CAS Registry Number.
103470-60-6Relevant articles and documents
Concise enantio- and diastereoselective total syntheses of fumagillol, RK-805, FR65814, ovalicin, and 5-demethylovalicin
Yamaguchi, Junichiro,Toyoshima, Maya,Shoji, Mitsuru,Kakeya, Hideaki,Osada, Hiroyuki,Hayashi, Yujiro
, p. 789 - 793 (2007/10/03)
(Chemical Equation Presented) L-Proline-mediated α-aminoxylation is a key step in the enantio- and diastereoselective total syntheses of fumagillin, ovalicin, and related compounds (see scheme). These compounds contain a cyclohexane ring, two epoxides, an
Total synthesis and absolute configuration of FR65814
Amano, Seiji,Ogawa, Noriko,Ohtsuka, Masami,Ogawa, Seiichiro,Chida, Noritaka
, p. 1263 - 1264 (2007/10/03)
The chiral and highly stereoselective synthesis of FR658141, a novel immunosuppressant, starting from D-glucose is described; this first total synthesis fully confirms the proposed structure of 1.