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2,3-Butanediol, 1-bromo-4-[(S)-(4-methylphenyl)sulfinyl]-, (2S,3S)is a chiral chemical compound with the molecular formula C10H13BrO2S. It features a butanediol backbone with a bromine atom and a sulfinyl group attached to it, specifically identified as a (S)-(4-methylphenyl)sulfinyl derivative of 2,3-butanediol. This white to light yellow solid at room temperature is commonly used as a reagent in organic synthesis and may have potential applications in the pharmaceutical or agrochemical industries, although further investigation is needed to determine its specific uses and properties.

503565-87-5

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503565-87-5 Usage

Uses

Used in Organic Synthesis:
2,3-Butanediol, 1-bromo-4-[(S)-(4-methylphenyl)sulfinyl]-, (2S,3S)is used as a reagent in organic synthesis for its unique structural features, including the bromine atom and the sulfinyl group, which can be utilized in various chemical reactions to form a range of products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3-Butanediol, 1-bromo-4-[(S)-(4-methylphenyl)sulfinyl]-, (2S,3S)may be employed as a building block or intermediate in the development of new drugs, given its chiral nature and the potential for further chemical modifications.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 2,3-Butanediol, 1-bromo-4-[(S)-(4-methylphenyl)sulfinyl]-, (2S,3S)could be used as a precursor or intermediate in the synthesis of agrochemicals, such as pesticides or herbicides, due to its unique chemical structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 503565-87-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,3,5,6 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 503565-87:
(8*5)+(7*0)+(6*3)+(5*5)+(4*6)+(3*5)+(2*8)+(1*7)=145
145 % 10 = 5
So 503565-87-5 is a valid CAS Registry Number.

503565-87-5Relevant academic research and scientific papers

A novel and stereospecific synthesis of (+)-exo-brevicomin

Raghavan, Sadagopan,Joseph, Suju C.

, p. 8237 - 8239 (2003)

A novel and stereospecific synthesis of (+)-exo-brevicomin is disclosed. The key step of the reaction sequence employs the sulfinyl moiety as an intramolecular nucleophile to functionalize an alkene π-complexed to a bromonium ion.

Stereoselective bromohydrin formation from β-hydroxy sulfoxides mediated by the pendant sulfoxide

Raghavan, Sadagopan,Abdul Rasheed,Joseph, Suju C.,Rajender

, p. 1845 - 1846 (1999)

Regio- and stereo-selective bromohydrin formation promoted by a neighbouring sulfinyl moiety is disclosed.

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