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(2R)-4-oxopiperidine-2-carboxylic acid ethyl ester is a chemical compound with the molecular formula C8H13NO3. It is an ethyl ester derivative of (2R)-4-oxopiperidine-2-carboxylic acid, characterized by its white solid appearance and a melting point of 86-87°C. (2R)-4-oxopiperidine-2-carboxylic acid ethyl ester is soluble in most organic solvents and is recognized for its utility as a building block in the synthesis of various pharmaceuticals and organic compounds.

357154-17-7

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357154-17-7 Usage

Uses

Used in Pharmaceutical Industry:
(2R)-4-oxopiperidine-2-carboxylic acid ethyl ester is used as a building block for the synthesis of various pharmaceuticals and organic compounds. Its role in the creation of biologically active compounds makes it a valuable precursor in the development of new medicines.
Used as a Reagent in Organic Synthesis:
In the field of organic chemistry, (2R)-4-oxopiperidine-2-carboxylic acid ethyl ester serves as a reagent, facilitating a range of chemical reactions that contribute to the synthesis of complex organic molecules. Its versatility in organic synthesis processes underscores its importance in the preparation of specialty chemicals and intermediates.

Check Digit Verification of cas no

The CAS Registry Mumber 357154-17-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,7,1,5 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 357154-17:
(8*3)+(7*5)+(6*7)+(5*1)+(4*5)+(3*4)+(2*1)+(1*7)=147
147 % 10 = 7
So 357154-17-7 is a valid CAS Registry Number.

357154-17-7Downstream Products

357154-17-7Relevant academic research and scientific papers

Practical synthesis of both enantiomers of protected 4-oxopipecolic acid

Machetti, Fabrizio,Cordero, Franca M,De Sarlo, Francesco,Brandi, Alberto

, p. 4995 - 4998 (2007/10/03)

A new synthesis of both enantiomers of protected 4-oxopipecolic acid was achieved in six steps via 1,3-dipolar cycloaddition of C-ethoxycarbonyl N-(1R)-phenylethylnitrone to but-3-en-1-ol.

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