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α-Methylbenzyl 4-chlorophenyl sulfone is an organic compound characterized by its molecular formula C14H13ClOS. It is a derivative of benzene, with a methyl group attached to the benzyl side chain and a 4-chlorophenyl sulfone group attached to the other end. α-methylbenzyl 4-chlorophenyl sulfone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. The compound is synthesized through a reaction between α-methylbenzyl chloride and 4-chlorophenol in the presence of a base, typically using a phase-transfer catalyst to facilitate the reaction. It is important to handle α-methylbenzyl 4-chlorophenyl sulfone with care due to its potential reactivity and the presence of a chlorine atom, which can contribute to environmental concerns if not managed properly.

24422-79-5

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24422-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24422-79-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,2 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24422-79:
(7*2)+(6*4)+(5*4)+(4*2)+(3*2)+(2*7)+(1*9)=95
95 % 10 = 5
So 24422-79-5 is a valid CAS Registry Number.

24422-79-5Downstream Products

24422-79-5Relevant academic research and scientific papers

Addition of 4-Chlorobenzenesulphenyl Chloride to 3-Methylbut-1-yne, Hex-1-yne, and Phenylacetylene: Isomerisation and Hydrolysis of the Adducts

Capozzi, Giuseppe,Romeo, Giovanni,Lucchini, Vittorio,Modena, Giorgio

, p. 831 - 836 (2007/10/02)

The addition of (4-ClC6H4SCl, (2), to RCH(*)CH, (1; R=Pri, Bun), gives (E)-4-ClC6H4(R)C(*)C(H)Cl, (E)-(3), and (E)-4-ClC6H4(H)C(*)C(R)Cl, (E)-(4) in a fixed ratio; the addition to (1; R=Ph) gives regiospecifically (E)-(3; R=Ph) in ethyl acetate, but different proportions of (E)-(3) and (E)-(4) (R=Ph), in chloroform, sym-tetrachloroethane, and acetic acid.With an excess of the sulphenyl chloride (2), (E)-(3) and (E)-(4) isomerize to (Z)-(4) (same R).The sulphuric-acid catalysed hydrolysis of (E)-(3; R=Pri, Bun, Ph) gives α-chloroketones RCOCH2Cl(5) (same R).The (E)-(4) isomers do not hydrolyse.

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