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82769-70-8

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82769-70-8 Usage

Description

(3S,4S)-2-Methyl-3-phenyl-4-((R)-toluene-4-sulfinyl)-isoxazolidine is a chiral isoxazolidine derivative characterized by a molecular formula of C15H19NO2S. It features a four-membered lactam ring with a phenyl and a methyl group attached, along with a sulfoxide group connected to a toluene moiety. (3S,4S)-2-Methyl-3-phenyl-4-((R)-toluene-4-sulfinyl)-isoxazolidine's unique structure and potential biological activity make it a promising candidate for pharmaceutical research and drug development.

Uses

Used in Pharmaceutical Research:
(3S,4S)-2-Methyl-3-phenyl-4-((R)-toluene-4-sulfinyl)-isoxazolidine is used as a research compound for exploring its potential biological activities and applications in the pharmaceutical industry. Its unique structure may offer novel insights and opportunities for the development of new drugs and therapies.
Used in Drug Development:
In the field of drug development, (3S,4S)-2-Methyl-3-phenyl-4-((R)-toluene-4-sulfinyl)-isoxazolidine is utilized as a key building block or molecular scaffold for the synthesis of new pharmaceutical agents. Its chiral nature and diverse functional groups may facilitate the creation of innovative drugs with improved efficacy and selectivity.
Used in Chemical Synthesis:
(3S,4S)-2-Methyl-3-phenyl-4-((R)-toluene-4-sulfinyl)-isoxazolidine serves as an intermediate in the synthesis of various complex organic molecules. Its unique structural features can be exploited to construct a wide range of compounds with potential applications in different industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Chiral Catalysts:
Due to its chiral nature, (3S,4S)-2-Methyl-3-phenyl-4-((R)-toluene-4-sulfinyl)-isoxazolidine may be employed as a chiral catalyst in asymmetric synthesis. This application could enhance the selectivity and yield of enantiomeric products, which are crucial in the production of single-enantiomer drugs with desired biological activities.
Used in Analytical Chemistry:
(3S,4S)-2-Methyl-3-phenyl-4-((R)-toluene-4-sulfinyl)-isoxazolidine can be utilized as a chiral reference standard or a resolving agent in analytical chemistry. Its distinct stereochemistry allows for the accurate determination of enantiomeric purity and the separation of chiral compounds in various analytical techniques, such as chromatography and spectroscopy.

Check Digit Verification of cas no

The CAS Registry Mumber 82769-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,6 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 82769-70:
(7*8)+(6*2)+(5*7)+(4*6)+(3*9)+(2*7)+(1*0)=168
168 % 10 = 8
So 82769-70-8 is a valid CAS Registry Number.

82769-70-8Relevant articles and documents

High Asymmetric Induction in the 1,3-Dipolar Cycloaddition of (R)-(+)-p-Tolyl Vinyl Sulfoxide with Acyclic Nitrones

Koizumi, Toru,Hirai, Hajime,Yoshii, Eiichi

, p. 4004 - 4005 (1982)

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