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2-Pyrrolidineacetic acid, methyl ester, (R)is a chiral chemical compound that is commonly used in the pharmaceutical industry. It is the methyl ester form of 2-pyrrolidineacetic acid, which is an amino acid derivative. 2-Pyrrolidineacetic acid, methyl ester, (R)is known for its specific spatial arrangement of atoms, making it a valuable component in the synthesis of pharmaceutical drugs, particularly those targeting the central nervous system.

61376-53-2

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61376-53-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Pyrrolidineacetic acid, methyl ester, (R)is used as a key intermediate in the synthesis of pharmaceutical drugs, particularly for those that target the central nervous system. Its unique chiral structure allows for the development of drugs with specific therapeutic effects.
Used in Neurological Disorder Treatment:
2-Pyrrolidineacetic acid, methyl ester, (R)is used as a potential treatment for various neurological disorders. Its role in modulating neurotransmitters makes it a promising candidate for the development of drugs that can alleviate symptoms and improve the quality of life for patients suffering from such conditions.
Used in Neurotransmitter Modulation Research:
2-Pyrrolidineacetic acid, methyl ester, (R)is used in research for its potential as a neurotransmitter modulator. Its ability to interact with neurotransmitters can lead to the development of new drugs that can effectively manage neurological conditions by influencing the communication between nerve cells.

Check Digit Verification of cas no

The CAS Registry Mumber 61376-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,7 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61376-53:
(7*6)+(6*1)+(5*3)+(4*7)+(3*6)+(2*5)+(1*3)=122
122 % 10 = 2
So 61376-53-2 is a valid CAS Registry Number.

61376-53-2Upstream product

61376-53-2Relevant academic research and scientific papers

Practical method for the synthesis of (R)-homopipecolinic acid and (R)-homoproline esters from ω-chloroalkanoic acids and available chiral amines

Hashimoto, Norio,Funatomi, Takashi,Misaki, Tomonori,Tanabe, Yoo

, p. 2214 - 2223 (2006)

A practical synthesis of (R)-homopipecolinic acid methyl ester 1 and (R)-homoproline methyl ester 2 was performed utilizing (i) a direct intramolecular cyclization of ω-chloro-β-enamino esters 11 and 12, which were prepared from available (S)-1-phenylethy

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