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α-Benzenesulfonyl-α-phenylpropionic acid is a chemical compound with the molecular formula C15H14O4S. It is a derivative of phenylpropionic acid, featuring a benzenesulfonyl group attached to the α-carbon. α-benzenesulfonyl-α-phenylpropionic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a chiral building block or intermediate. It is characterized by its ability to form salts and esters, which can be used in the development of drugs with specific therapeutic properties. The compound's structure allows for a range of chemical reactions, making it a versatile component in organic synthesis.

51416-86-5

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51416-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51416-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,1 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51416-86:
(7*5)+(6*1)+(5*4)+(4*1)+(3*6)+(2*8)+(1*6)=105
105 % 10 = 5
So 51416-86-5 is a valid CAS Registry Number.

51416-86-5Relevant academic research and scientific papers

Decarboxylative allylation using sulfones as surrogates of alkanes

Weaver, Jimmie D.,Tunge, Jon A.

supporting information; experimental part, p. 4657 - 4660 (2009/05/13)

(Chemical Equation Presented) α-Sulfonyl functional groups are traceless activating groups that facilitate catalytic decarboxylative allylations in high yield yet can be cleaved to allow the synthesis of simple allylated alkanes. Substrate studies suggest

New decarboxylative sulfanylation of some phenylsulfonyl arylacetic acids

Wladislaw, Blanka,Marzorati, Liliana,Di Vitta, Claudio,Claro, Nelson F.

, p. 1 - 7 (2007/10/03)

The reaction of some α-phenylsulfonyl arylacetic acids with NaH in DMSO and dimethyl disulfide leading to α-sulfanylated benzyl phenyl sulfones is discussed.

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