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6290-95-5

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6290-95-5 Usage

General Description

[(3-bromobutan-2-yl)sulfonyl]benzene is a chemical compound with the molecular formula C10H13BrO2S. It consists of a benzene ring with a sulfonyl group attached to it, and a 3-bromobutan-2-yl group attached to the sulfonyl group. [(3-bromobutan-2-yl)sulfonyl]benzene is used in organic synthesis, particularly in the formation of sulfones and sulfonyl chlorides. It has also been studied for its potential use in pharmaceutical applications and as a starting material for the synthesis of various organic compounds. Overall, [(3-bromobutan-2-yl)sulfonyl]benzene is an important building block in organic chemistry with various potential applications.

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.

6290-95-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromobutan-2-ylsulfonylbenzene

1.2 Other means of identification

Product number -
Other names [(3-bromobutan-2-yl)sulfonyl]benzene

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 -
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More Details:6290-95-5 SDS

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.

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