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(S)-4-(4-Fluoro-phenyl)-2-hydroxy-3,3-dimethyl-4-oxo-butyric acid ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

474385-91-6

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474385-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 474385-91-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,3,8 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 474385-91:
(8*4)+(7*7)+(6*4)+(5*3)+(4*8)+(3*5)+(2*9)+(1*1)=186
186 % 10 = 6
So 474385-91-6 is a valid CAS Registry Number.

474385-91-6Upstream product

474385-91-6Downstream Products

474385-91-6Relevant academic research and scientific papers

C(2)-symmetric Sc(III)-complexes as chiral Lewis acids. Catalytic enantioselective aldol additions to glyoxylate esters.

Evans, David A,Masse, Craig E,Wu, Jimmy

, p. 3375 - 3378 (2002)

Cationic Lewis acid complexes [Sc(pyridyl-bis(oxazolinyl)](Cl(2))SbF(6) 1a and 1b catalyze aldol reactions with ethyl glyoxylate with enantioselectivities ranging from 90 to 99% ee and syn reaction diastereoselections ranging from 90:10 to 95:5. [reaction: see text]

A general method for the enantioselective synthesis of pantolactone derivatives

Evans, David A.,Wu, Jimmy,Masse, Craig E.,MacMillan, David W. C.

, p. 3379 - 3382 (2007/10/03)

(matrix presented) An efficient enantioselective synthesis of β,β-dialkyl-γ-substituted pantolactones has been achieved utilizing the cationic [Sc((S,S)-R-pybox)]-(Cl)2+, R = Ph (9), t-Bu (10), complex in a catalyzed aldol reaction as the key step. The pantolactone derivatives are isolated in enantiomeric excesses.

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