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(R)-(+)-α-n-butyl-β-aminopropionic acid, also known as L-4-aminopipecolic acid, is a chiral amino acid derivative with the molecular formula C8H17NO2. It features an α-aminopropionic acid group and a butyl group, and due to its single chiral center, it exists as a pair of enantiomers. The (R)-(+)-enantiomer exhibits specific optical properties and is utilized in the synthesis of pharmaceuticals, serving as a reagent in organic chemistry, and has been investigated for its potential impact on neurotransmitter systems in the brain.

183182-05-0

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183182-05-0 Usage

Uses

Used in Pharmaceutical Synthesis:
(R)-(+)-α-n-butyl-β-aminopropionic acid is used as a key intermediate in the synthesis of various pharmaceuticals for [application reason, e.g., its unique structural properties that can be leveraged in drug design].
Used in Organic Chemistry:
In the field of organic chemistry, (R)-(+)-α-n-butyl-β-aminopropionic acid is used as a reagent for [application reason, e.g., facilitating specific chemical reactions or providing a source of the amino acid in various chemical processes].
Used in Neurotransmitter Research:
(R)-(+)-α-n-butyl-β-aminopropionic acid is used as a research compound to study its potential effects on neurotransmitter systems in the brain, with the aim of [application reason, e.g., developing new treatments for neurological disorders or understanding brain chemistry].

Check Digit Verification of cas no

The CAS Registry Mumber 183182-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,1,8 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 183182-05:
(8*1)+(7*8)+(6*3)+(5*1)+(4*8)+(3*2)+(2*0)+(1*5)=130
130 % 10 = 0
So 183182-05-0 is a valid CAS Registry Number.

183182-05-0Downstream Products

183182-05-0Relevant academic research and scientific papers

Enantioselective synthesis of β-amino acids. 7. Preparation of enantiopure α-substituted β-amino acids from 1-benzoyl-2(S)-tert-butyl-3-methylperhydropyrimidin-4-one

Juaristi, Eusebio,Quintana, Delia,Balderas, Margarita,Garcia-Perez, Enrique

, p. 2233 - 2246 (2007/10/03)

Inexpensive natural α-amino acid L-asparagine was efficiently converted to either (R)- or (S)-α-alkylated β-amino acids in enantiomerically pure state. The key intermediate in this protocol is the enantiopure N,N-acetal pyrimidinone (S)-1, a masked chiral derivative of β-alanine.

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