21134-15-6

Usage

Appearance

White to off-white solid.

Solubility

Insoluble in water, soluble in organic solvents.

Uses

Building block in the synthesis of various pharmaceuticals and agrochemicals.

Potential Applications

Corrosion inhibitor, precursor for the synthesis of dyes and polymers.

Safety Precautions

Harmful if ingested or inhaled, may cause skin and eye irritation, handle with care.

InChI:InChI=1/C13H12O3S/c1-17(14,15)13-9-7-12(8-10-13)16-11-5-3-2-4-6-11/h2-10H,1H3

Upstream product

• 14763-60-1 4-methanesulfonyl-phenol 
• 98-80-6 phenylboronic acid 
• 38778-05-1 4-(Phenoxy)benzenethiol 
• 3466-32-8 4-bromoohenyl methyl sulfone 
• 108-95-2 phenol 
• 18052-27-2 tert-butyldimethyl(phenoxy)silane 
• 21134-14-5 methyl (4-phenyloxy)phenyl sulfide 
• 101-84-8 diphenylether 
• 6462-31-3 methyl 2,4,6-trimethylphenyl sulfone 

Downstream Products

• 866553-34-6 2-benzyloxycarbonylamino-3,3,3-trifluoro-2-(4-phenoxy-benzenesulfonylmethyl)-propionic acid ethyl ester 
• 83642-22-2 1-(4-(4-(methylsulfonyl)phenoxy)phenyl)ethanone 
• 83642-23-3 (4-(4-(methylsulfonyl)phenoxy)phenyl)phenylmethanone 
• 83642-32-4 4-(4-methylsulfonylphenoxy)phenylsulfonyl chloride 
• 866553-36-8 [1-benzyloxycarbamoyl-2,2,2-trifluoro-1-(4-phenoxy-benzenesulfonylmethyl)-ethyl]-carbamic acid benzyl ester 
• 866553-38-0 2-(benzyloxycarbonyl-methyl-amino)-3,3,3-trifluoro-2-(4-phenoxy-benzenesulfonylmethyl)-propionic acid ethyl ester 
• 866553-35-7 2-benzyloxycarbonylamino-3,3,3-trifluoro-2-(4-phenoxy-benzenesulfonylmethyl)-propionic acid 

Relevant academic research and scientific papers

Rhodium-catalyzed direct ortho-alkenylation of phenyl sulfones with alkynes utilizing sulfonyl function as modifiable directing group

Abstract The ortho-selective alkenylation of phenyl sulfones with alkynes proceeds effectively in the presence of a cationic Cp?-rhodium(III) catalyst together with an appropriate carboxylic acid involving regioselective C-H bond cleavage directed by the sulfonyl function. An (ortho-alkenylated phenyl) methyl sulfone prepared by this hydroarylation method undergoes palladium-catalyzed α-arylation and subsequent diastereoselective cyclization to directly produce the corresponding thiochromane 1,1-dioxide derivatives.

Synthesis of α-trifluoromethyl-α-amino-β-sulfone hydroxamates: Novel nanomolar inhibitors of matrix metalloproteinases

The racemic α-trifluoromethyl-α-amino-β-sulfone hydroxamates 1 were synthesized by means of a nucleophilic addition of sulfur-stabilized carbanions to a N-Cbz imine of trifluoropyruvate (4). The free amino derivative 1a was the most potent inhibitor of both MMP-3 (stromelysin-1) and MMP-9 (gelatinase-B), showing an IC50 = 14 nM and 1 nM, respectively, and excellent selectivity versus MMP-1 (>5000-fold difference in inhibitory capacity). The N-Me derivative 1b was the most selective for MMP-3 with respect to MMP-9 (62-fold difference).

A general and efficient protocol for the synthesis of biaryl ethers from aryl silyl ethers using Cs2CO3

A general and efficient one-step procedure has been developed for the synthesis of biaryl ethers via direct coupling of electron-deficient arylhalides or aryl triflates to aryl t-butyldimethylsilyl (TBS) ethers using Cs 2CO3. The protocol was also applied to electron-rich arylhalides by addition of a catalytic amount of copper(I) iodide. The reaction is rapid and provides good to excellent yields.

HYDROXAMIC ACID DERIVATIVE AND MMP INHIBITOR CONTAINING THE SAME AS ACTIVE INGREDIENT

A hydroxamic acid derivative represented by the following general formula (1) having selective MMP inhibitory activity, , wherein R1 andR2 each represents hydrogen atom, lower alkyl group, lower haloalkyl etc., X represents methylene

Transsulfonylation between Aromatic Sulfones and Arenes.

Transsulfonylation between various aromatic and arenes catalyzed by triflic acid at 150 deg C are described.The structural requirements for the occurence of the transsulfonylations are shown to be similar to those for the transacylations that were described earlier.However, in view of the inherent differences in the properties of aromatic ketones and sulfones with respect to conjugation of the carbonyl and sulfonyl groups with the aromatic ring, a different rationale for the transsulfonylation reactions is offered.A mechanism is suggested that rationalizes the similar structural requirements for transacylations in terms of steric relief of strain in the reactions of certain ketones and sulfones.