6290-95-5 Usage
Description
[(3-bromobutan-2-yl)sulfonyl]benzene is a chemical compound characterized by the molecular formula C10H13BrO2S. It features a benzene ring with a sulfonyl group attached, and a 3-bromobutan-2-yl group connected to the sulfonyl moiety. [(3-bromobutan-2-yl)sulfonyl]benzene serves as a significant building block in organic chemistry due to its versatile structure and reactivity.
Uses
Used in Organic Synthesis:
[(3-bromobutan-2-yl)sulfonyl]benzene is utilized as an intermediate in the synthesis of various organic compounds, particularly in the formation of sulfones and sulfonyl chlorides. Its unique structure allows for further functionalization and modification, making it a valuable component in the creation of complex molecules.
Used in Pharmaceutical Applications:
[(3-bromobutan-2-yl)sulfonyl]benzene has been investigated for its potential use in the pharmaceutical industry. Its specific properties, such as the presence of the sulfonyl group and the bromine atom, may contribute to the development of new drugs or drug candidates with novel therapeutic properties.
Used as a Starting Material:
[(3-bromobutan-2-yl)sulfonyl]benzene also serves as a starting material for the synthesis of a wide range of organic compounds. Its reactivity and structural features make it an attractive candidate for use in the development of new chemical entities with potential applications in various fields, including materials science, agrochemistry, and the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 6290-95-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6290-95:
(6*6)+(5*2)+(4*9)+(3*0)+(2*9)+(1*5)=105
105 % 10 = 5
So 6290-95-5 is a valid CAS Registry Number.
6290-95-5Relevant articles and documents
Stereochemistry of Free-Radical Eliminations on β-Phenylsulfonyl Radicals
Boothe, Thomas E.,Greene, Joseph L.,Shevlin, Philip B.
, p. 794 - 797 (2007/10/02)
Tributyltin radicals have been allowed to react with erythro- and threo-2-bromo-3-(phenylsulfonyl)butane (5a,b) to generate β-(phenylsulfonyl)-sec-butyl radicals 9.The intermediate 9 eliminates phenylsulfonyl radicals to form 2-butenes in a nonstereospecific manner.The lack of stereospecificity is due to rotation about the C2-C3 bond before the loss of the phenylsulfonyl radical can occur and implies that the stabilization of the radical by sulfur bridging is negligible.
