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acetic acid (R)-2-phenylsulfonyl-1-methylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

862249-93-2

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862249-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 862249-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,2,4 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 862249-93:
(8*8)+(7*6)+(6*2)+(5*2)+(4*4)+(3*9)+(2*9)+(1*3)=192
192 % 10 = 2
So 862249-93-2 is a valid CAS Registry Number.

862249-93-2Relevant academic research and scientific papers

Synthesis of a novel ruthenium(I{cyrillic, ukrainian}I{cyrillic, ukrainian}) complex and its unique behaviors in enzymatic dynamic kinetic resolution of secondary alcohols

Chen, Qihui,Yuan, Chengye

experimental part, p. 3707 - 3716 (2010/07/05)

A cyclopentadienyl benzoyl ruthenium(I{cyrillic, ukrainian}I{cyrillic, ukrainian}) complex 3 was first prepared as an efficient catalyst in Candida Antarctica lipase B (CALB) mediated dynamic kinetic resolution (DKR) of secondary alcohols. With the aid of this ruthenium complex 3, (S)-1-phenylethanol was completely racemized within 25 min, and in combination with CALB, series of secondary alcohols bearing various functional groups were resolved in an efficient DKR manner. A detailed mechanism involving the C-H bond activation was presented for the formation of complex 3 by capturing the crucial intermediate in this pathway. Related mechanistic studies were carried out to illustrate this type of DKR catalyst is based on the racemization of secondary alcohols. The novelty of its structure, its unique catalytic behavior as well as its wide scope of application of various substrates and its higher efficiency make complex 3 as an important alternative to those complexes, which are commonly used in DKR process.

Lipase-promoted dynamic kinetic resolution of racemic β-hydroxyalkyl sulfones

Kielbasinski, Piotr,Rachwalski, Michal,Mikolajczyk, Marian,Moelands, Marcel A. H.,Zwanenburg, Binne,Rutjes, Floris P. J. T.

, p. 2157 - 2160 (2007/10/03)

A series of racemic aryl β-hydroxyalkyl sulfones have been successfully transformed into the corresponding optically active O-acetyl derivatives in high yields (up to 80%) with enantiomeric excesses more than 99% using a dynamic kinetic resolution procedure, in which a lipase-promoted kinetic resolution is combined with a concomitant ruthenium-catalysed racemization of the substrates.

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