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103470-60-6

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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.

103470-60-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-methyl-3-(3-methylbut-2-enyl)oxiran-2-yl]-1-oxaspiro[2.5]octane-5,6-diol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:103470-60-6 SDS

103470-60-6Downstream Products

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.

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