34622-39-4 Usage
Description
(S)-2-PIPERIDINONE-6-CARBOXYLIC ACID, also known as (S)-6-Oxo-2-piperidinecarboxylic acid, is an organic compound that serves as a key intermediate in the synthesis of various pharmaceutical compounds and metabolites. It is characterized by its unique chemical structure, which allows it to participate in a range of reactions and contribute to the development of novel therapeutic agents.
Uses
Used in Pharmaceutical Synthesis:
(S)-2-PIPERIDINONE-6-CARBOXYLIC ACID is used as a reactant for the synthesis of various metabolites of lysine, which are developed during aging and in diabetic patients. These metabolites play a crucial role in understanding the metabolic changes associated with these conditions and can potentially lead to the development of new treatments.
Used in the Synthesis of Functionalized β-lactam N-heterocycles:
(S)-2-PIPERIDINONE-6-CARBOXYLIC ACID is used as a reactant for the synthesis of functionalized β-lactam N-heterocycles via carboxymethylproline synthase catalyzed cyclization reactions. These compounds have potential applications in the development of new antibiotics and other therapeutic agents.
Used in the Synthesis of Pro-(S)-C5 branched [4.3.1] aza-amide bicycles:
(S)-2-PIPERIDINONE-6-CARBOXYLIC ACID is used as a reactant to synthesize Pro-(S)-C5 branched [4.3.1] aza-amide bicycles, which are potential inhibitors for FK506-binding proteins. These inhibitors can be utilized in the development of immunosuppressive drugs and other therapeutic agents targeting protein-protein interactions.
Used in the Synthesis of Ethyl (S)-2-(6-oxopiperidin-2-yl)acetate:
(S)-2-PIPERIDINONE-6-CARBOXYLIC ACID is used as a reactant to synthesize Ethyl (S)-2-(6-oxopiperidin-2-yl)acetate, which can be reduced using LiBH4 to produce optically pure hydroxymethyl lactams. These hydroxymethyl lactams have potential applications in the development of various pharmaceutical compounds, including those with analgesic, anti-inflammatory, and anti-cancer properties.
Check Digit Verification of cas no
The CAS Registry Mumber 34622-39-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,6,2 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34622-39:
(7*3)+(6*4)+(5*6)+(4*2)+(3*2)+(2*3)+(1*9)=104
104 % 10 = 4
So 34622-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO3/c8-5-3-1-2-4(7-5)6(9)10/h4H,1-3H2,(H,7,8)(H,9,10)/t4-/m0/s1
34622-39-4Relevant articles and documents
THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE
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Page/Page column, (2015/02/19)
Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.
THERAPEUTICALLY ACTIVE COMPOUNDS AND THEIR METHODS OF USE
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Page/Page column 93, (2015/02/19)
Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.
THERAPEUTICALLY ACTIVE COMPOSITIONS AND THEIR METHODS OF USE
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Page/Page column, (2013/07/31)
Provided are methods of treating a cancer characterized by the presence of a mutant allele of IDH1/2 comprising administering to a subject in need thereof a compound described here.
