103470-60-6 Usage
General Description
The chemical compound (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 spirocyclic structure. It contains two epoxide (oxiran) rings, one of which is attached to a methyl group and a double bond. The compound 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. (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 likely has potential applications in organic synthesis, medicinal chemistry, and biochemical research due to its unique structure and functional groups.
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.