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(R)-1-(p-chlorophenyl)-2-methylpropanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

137491-92-0

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137491-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137491-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,4,9 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 137491-92:
(8*1)+(7*3)+(6*7)+(5*4)+(4*9)+(3*1)+(2*9)+(1*2)=150
150 % 10 = 0
So 137491-92-0 is a valid CAS Registry Number.

137491-92-0Downstream Products

137491-92-0Relevant academic research and scientific papers

Application of well-defined chain-end-functionalized polystyrenes with dendritic chiral ephedrine moieties as reagents for highly catalytic enantioselective addition of dialkylzincs to aldehydes

El-Shehawy, Ashraf A.,Sugiyama, Kenji,Hirao, Akira

, p. 425 - 434 (2008)

A series of well-defined chain-end-functionalized polystyrenes having a definite number of chiral ephedrine moieties dendritically distributed at the periphery of their hyperbranched chain-ends were evaluated as chiral catalysts for the enantioselective addition of dialkylzinc reagents to aldehydes. These dendritic macromolecules worked well as homogeneous chiral catalysts and exhibited high catalytic activity and enantioselectivity very similar to those observed for the corresponding monomeric chiral catalysts. The optimum amount of chiral catalyst was found to be 5 mol %. A profound number effect of the chiral ephedrine moieties was observed, and PS(Ephed)8 having eight chiral ephedrine moieties at the periphery was found to be superior to other dendritic chiral catalysts. The enantioselectivity reached a value of 95% in the addition of diisopropylzinc to 3-phenylpropanal. The dendritic chiral catalysts could be easily recovered from the reaction solution by using a solvent precipitation method, and the recovered catalyst showed no significant loss of its catalytic activity or enantioselectivity.

Facile synthesis of chiral isopropyl carbinols with high enantiomeric excess via catalytic enantioselective addition of diisopropylzinc to aldehydes

Yang, Weon Ki,Cho, Byung Tae

, p. 2947 - 2953 (2007/10/03)

Highly effective syntheses of chiral alkyl and aryl isopropyl carbinols with high enantiomeric excess (94-98% ee) via catalytic enantioselective addition of diisopropylzinc to aldehydes have been developed.

Synthesis of chiral 1-arylalkan-1-ols using crude enzymes

Basavaiah,Raju

, p. 1859 - 1863 (2007/10/02)

Enantioselective hydrolysis of racemic 1-acetoxy-1-aryl-alkanes has been examined by two selected enzymes, crude pig liver acetone powder and crude goat liver acetone powder, providing 1-arylalkan-1-ols in high optical purities.

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