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ethyl 2-(4-chlorophenyl)-2-hydroxypropionate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100126-96-3

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100126-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100126-96-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,2 and 6 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100126-96:
(8*1)+(7*0)+(6*0)+(5*1)+(4*2)+(3*6)+(2*9)+(1*6)=63
63 % 10 = 3
So 100126-96-3 is a valid CAS Registry Number.

100126-96-3Relevant academic research and scientific papers

α-Fluoro analogues of inflammation inhibiting α-arylpropionic acids

Schlosser, Manfred,Michel, Dominique,Guo, Zhi-Wei,Sih, Charles J.

, p. 8257 - 8262 (1996)

2-Aryl-2-fluoropropionic acids were prepared by treatment of either ethyl α-hydroxy-carboxylates or cyanohydrin O-silyl ethers with diethylaminosulfur trifluoride and subsequent hydrolysis. The methyl ester of 2-fluoro-2-(4- isobutylphenyl)propionic acid

Highly homogeneous stereocontrolled construction of quaternary hydroxyesters by addition of dimethylzinc to α-ketoesters promoted by chiral perhydrobenzoxazines and B(OEt)3

Infante, Rebeca,Nieto, Javier,Andres, Celia

, p. 4375 - 4379 (2012/05/20)

A highly efficient enantioselective addition of Me2Zn to α-ketoesters, assisted by a chiral perhydro-1,3-benzoxazine ligand, is described. This novel catalytic system offers homogeneous elevated enantioselectivities in the preparation of α-hydroxyesters that bear a quaternary stereocenter, with a minor dependence on electronic and steric effects when aromatic, heteroaromatic, or aliphatic α-ketoesters are employed. The catalyst can be recovered and reused without loss of activity.

Propargylether derivatives

-

, (2008/06/13)

Propargylether derivatives of formula I including the optical isomers thereof and mixtures of such isomers, wherein R1is hydrogen, alkyl, cycloalkyl or optionally substituted aryl, R2and R3are each independently hydrogen o

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