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2-((R)-Naphthalene-1-sulfinyl)-1-phenyl-ethanol is a complex organic compound characterized by its unique molecular structure. It features a chiral center, indicated by the "R" prefix, which specifies the configuration of the molecule as the right-handed version in a stereochemical sense. The compound consists of a naphthalene ring, which is a fused pair of benzene rings, with a sulfinyl group (-SO) attached to the first carbon. This is connected to a phenyl group (a benzene ring) and an ethanol moiety (a two-carbon chain with a hydroxyl group). This specific arrangement of functional groups gives the compound its distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

93273-71-3

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93273-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93273-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,7 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93273-71:
(7*9)+(6*3)+(5*2)+(4*7)+(3*3)+(2*7)+(1*1)=143
143 % 10 = 3
So 93273-71-3 is a valid CAS Registry Number.

93273-71-3Downstream Products

93273-71-3Relevant academic research and scientific papers

INFLUENCE DE LA NATURE DU LIGAND AROMATIQUE SUR L'INDUCTION ASYMETRIQUE OBSERVEE LORS DE L'ADDITION D'ARYLMETHYLSULFOXYDES SUR DES CARBONYLES

Demailly, Gilles,Greck, Christine,Solladie, Guy

, p. 4113 - 4116 (2007/10/02)

The presence of an orthopyridyl substituent instead of a p-Tolyl on a chiral sulfoxide group increased drastically the asymmetric induction observed during the addition of arylmethylsulfoxide on carbonyl compounds.

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