123912-78-7

Basic information

• Product Name: 2-PYRROLIDIN-1-YL-PROPIONIC ACID
• Synonyms: TIMTEC-BB SBB010295;2-PYRROLIDIN-1-YL-PROPIONIC ACID;AKOS BC-0364;CHEMBRDG-BB 4401695;2-pyrrolidin-1-ylpropanoic acid hydrochloride;1-pyrrolidineacetic acid, alpha-methyl-;2-pyrrolidin-1-ylpropanoic acid(SALTDATA: 0.3H2O);2-pyrrolidin-1-ylpropanoic acid 0.3H2O
• CAS NO: 123912-78-7
• Molecular Formula: C₇H₁₃NO₂
• Molecular Weight: 143.18
• Mol File: 123912-78-7.mol

Chemical Properties

• Boiling Point: 240.6°C at 760 mmHg
• Flash Point: 99.3°C
• Appearance: /
• Density: 1.131g/cm³
• Vapor Pressure: 0.0126mmHg at 25°C
• Refractive Index: 1.503
• Storage Temp.: 2-8°C
• PKA: 2.56±0.10(Predicted)
• CAS DataBase Reference: 2-PYRROLIDIN-1-YL-PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PYRROLIDIN-1-YL-PROPIONIC ACID(123912-78-7)
• EPA Substance Registry System: 2-PYRROLIDIN-1-YL-PROPIONIC ACID(123912-78-7)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• HazardClass: IRRITANT
• Hazardous Substances Data: 123912-78-7(Hazardous Substances Data)

Usage

Uses

Used in Cognitive Enhancement:
Piracetam is used as a cognitive enhancer to improve learning and memory. It facilitates the activity of neurotransmitters in the brain, leading to enhanced cognitive function and mental performance.
Used in Neuroprotection:
Piracetam is used for its neuroprotective properties, potentially offering protection against brain damage and age-related cognitive decline. This makes it a valuable supplement for individuals concerned about maintaining their cognitive health as they age.
Used in Dietary Supplements Industry:
In the dietary supplements industry, piracetam is used as a key ingredient in products designed to enhance cognitive abilities and support brain health. Its safety and efficacy make it a popular choice for consumers looking to improve their mental performance and overall cognitive well-being.

InChI:InChI=1/C7H13NO2/c1-6(7(9)10)8-4-2-3-5-8/h6H,2-5H2,1H3,(H,9,10)

Upstream product

• 26846-86-6 (pyrrolidinyl-1)-2 propanoate d'ethyle 

Relevant articles and documents

Iodine-mediated direct α-amination of dimethyl methylmalonate using non-protected amines

In this study, direct C[sbnd]N bond formation was achieved via the reaction of a dimethyl methylmalonate with various amines in the presence of molecular iodine to produce α-aminocarbonyl compounds. This versatile methodology of the α-amination of a carbonyl-containing compound involves the in situ iodination of the dimethyl methylmalonate, thus promoting the formation of its enolate isomer, which then facilitates its nucleophilic substitution reaction with an amine. This strategy is highly practical and can be used in industry due to its requirement of only readily available reagents without any pre-preparation of the amines and other substrates.

1,2-NAPHTHOQUINONE DERIVATIVE AND METHOD FOR PREPARING SAME

Disclosed are a compound represented by Formula (1), or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, tautomer, enantiomer, or pharmaceutically acceptable diastereomer thereof, a method of preparing the same, and a pharmaceutical composition, which have effects for treatment or prevention of metabolic syndromes, comprising the same: wherein R1to R6, X1 to X4, and n are the same as defined in Claim 1.