1380547-40-9 Usage
Description
(±)-2-pivalamidopentanoic acid, also known as 2-PAPA, is a racemic mixture of two enantiomers of 2-pivalamidopentanoic acid. It is a derivative of valproic acid, a medication used to treat epilepsy, bipolar disorder, and migraines. 2-PAPA possesses potential anticonvulsant properties and is being studied for its possible applications in the pharmaceutical industry.
Used in Pharmaceutical Industry:
(±)-2-pivalamidopentanoic acid is used as a potential treatment for epilepsy due to its anticonvulsant effects, which are similar to those of valproic acid. It is being investigated for its efficacy in managing seizures and seizure-related disorders.
Used in Synthesis of Pharmaceuticals:
(±)-2-pivalamidopentanoic acid is used as a building block in the synthesis of various pharmaceuticals. Its unique structure allows it to be incorporated into the development of new medications with potential therapeutic benefits.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
(±)-2-pivalamidopentanoic acid is used as a chiral auxiliary in asymmetric synthesis. This application is crucial for the production of enantiomerically pure compounds, which are essential in the pharmaceutical industry to ensure the desired biological activity and minimize side effects.
Further research is necessary to fully understand the potential applications and effects of (±)-2-pivalamidopentanoic acid, as its role in the treatment of epilepsy and other uses is still being explored.
Check Digit Verification of cas no
The CAS Registry Mumber 1380547-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,0,5,4 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1380547-40:
(9*1)+(8*3)+(7*8)+(6*0)+(5*5)+(4*4)+(3*7)+(2*4)+(1*0)=159
159 % 10 = 9
So 1380547-40-9 is a valid CAS Registry Number.
1380547-40-9Relevant articles and documents
Catalytic asymmetric synthesis of functionalized α,α- disubstituted α-amino acid derivatives from racemic unprotected α-amino acids via in-situ generated azlactones
Weber, Manuel,Frey, Wolfgang,Peters, Rene
, p. 1443 - 1449 (2012)
Masked and activated highly enantioenriched α,α-disubstituted α-amino acids with an additional adjacent stereocenter were formed by a tandem reaction involving five steps using racemic unprotected amino acid substrates. Key step is the 1,4-addition of in-situ generated azlactones to a broad number of enones. The products of this step-economic route can, e.g., be useful for a divergent and rapid access to biologically interesting unnatural glutamic acid derivatives. Copyright
