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(2R,4S)-4-Ethyl-piperidine-2-carboxylic acid is a chemical compound with the molecular formula C9H17NO2. It is a derivative of piperidine, a heterocyclic organic compound that is commonly used as a building block in organic synthesis. The (2R,4S) stereochemistry designation indicates the spatial arrangement of the molecule's atoms, particularly the two chiral carbons found in the piperidine ring. (2R,4S)-4-Ethyl-piperidine-2-carboxylic acid has potential pharmaceutical applications due to its structural resemblance to neurotransmitters and its ability to interact with biological systems. Additionally, its carboxylic acid functional group makes it an important intermediate in the production of various pharmaceuticals and agrochemicals.

79415-24-0

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79415-24-0 Usage

Uses

Used in Pharmaceutical Industry:
(2R,4S)-4-Ethyl-piperidine-2-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its structural similarity to neurotransmitters allows it to potentially modulate the activity of these signaling molecules, making it a promising candidate for the development of drugs targeting neurological disorders.
Used in Agrochemical Industry:
(2R,4S)-4-Ethyl-piperidine-2-carboxylic acid is also used as an intermediate in the production of agrochemicals. Its carboxylic acid functional group can be utilized to create compounds that can interact with biological systems in plants and animals, potentially leading to the development of new pesticides or other agricultural products.

Check Digit Verification of cas no

The CAS Registry Mumber 79415-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,1 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 79415-24:
(7*7)+(6*9)+(5*4)+(4*1)+(3*5)+(2*2)+(1*4)=150
150 % 10 = 0
So 79415-24-0 is a valid CAS Registry Number.

79415-24-0Relevant academic research and scientific papers

An Improved Synthesis of Homoproline and Derivatives

Shuman, Robert T.,Ornstein, Paul L.,Paschal, Jonathan W.,Gesellchen, Paul D.

, p. 738 - 741 (2007/10/02)

An improved, general synthesis of substituted homoprolines has been developed by using readily available substituted pyridines (1).A key step in this synthetic procedure involves the known conversion of pyridine-N-oxides to 2-cyanopyridines (3) in nearly quantitative yields.The resulting nitriles are hydrolyzed to the corresponding pyridine-2-carboxylic acids (4).Subsequent reduction of the aromatic ring with PtO2/H2 gives the homoprolines (5) in good yields as racemic cis isomers.This procedure also can be utilized for the preparation of 5,6-benzohomoprolines fromthe appropriate quinoline precursors.The N-tert-butyloxycarbonyl (Boc) derivatives of these amino acids (useful intermediates for peptide synthesis) were also prepared in good yields.

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