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(1RS,2SR)-1-phenyl-2-(methylthio)propanol is a chiral organic compound characterized by its unique structure, consisting of a phenyl group attached to the first carbon, a methylthio group on the second carbon, and a hydroxyl group on the third carbon. (1RS,2SR)-1-phenyl-2-(methylthio)propanol is a specific stereoisomer, with the R configuration at both the first and second carbon atoms. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly those containing chiral centers. The compound's properties, such as its optical activity and reactivity, are influenced by its stereochemistry, making it a valuable building block in the development of enantiomerically pure compounds.

7715-10-8

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7715-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7715-10-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7715-10:
(6*7)+(5*7)+(4*1)+(3*5)+(2*1)+(1*0)=98
98 % 10 = 8
So 7715-10-8 is a valid CAS Registry Number.

7715-10-8Downstream Products

7715-10-8Relevant academic research and scientific papers

Enantioselective Oxidation of β-Hydroxythioethers. Synthesis of Optically Active Alcohols and Epoxides

Conte, V.,Furia, F. Di,Licini, G.,Modena, G.,Sbampato, G.,Valle, G.

, p. 257 - 276 (2007/10/02)

Optically pure β-hydroxysulfoxides may be obtained by direct oxidation of the parent thioethers with the modified Sharpless reagent developed in our laboratory.Necessary requisites for a successful asymmetric oxidation are both the protection of the OH function and the largest possible difference in size of the two groups linked to the thioether sulfur.This latter condition is fulfilled by using S-methyl derivatives.Examples referring to the oxidation of various S-methyl-β-hydroxythioethers, characterized by e.e. values up to 80percent, which may be further increased (>98percent) by crystallization, are presented.Results concerning the synthesis of optically active epoxides and alcohols starting from β-hydroxysulfoxides are also presented which, in some cases, allows the absolute configuration of the parent sulfoxide to be established.

Asymmetric Oxidation of Thioethers. Enantioselective Synthesis of β-Hydroxysulfoxides by Direct Oxidation

Conte, Valeria,Furia, Fulvio Di,Licini, Giulia,Modena, Giorgio

, p. 4859 - 4862 (2007/10/02)

S-methyl β-hydroxysulfoxides of fairly high optical purity (up to 80percent) may be prepared by direct asymmetric oxidation of acetylated or silylated S-methyl β-hydroxysulfides and subsequent deprotection.The upgrading of t

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