88016-17-5

Basic information

• Product Name: 2-Pyrrolidinone,4-amino-(9CI)
• Synonyms: 2-Pyrrolidinone,4-amino-(9CI);4-amino-2-Pyrrolidinone;4-AMinopyrrolidin-2-one
• CAS NO: 88016-17-5
• Molecular Formula: C4H8N2O
• Molecular Weight: 100.12
• Product Categories: VARIOUSAMINE
• Mol File: 88016-17-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 305.589 °C at 760 mmHg
• Flash Point: 138.616 °C
• Appearance: /
• Density: 1.127 g/cm³
• Storage Temp.: 2-8°C(protect from light)
• PKA: 15.92±0.40(Predicted)
• CAS DataBase Reference: 2-Pyrrolidinone,4-amino-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyrrolidinone,4-amino-(9CI)(88016-17-5)
• EPA Substance Registry System: 2-Pyrrolidinone,4-amino-(9CI)(88016-17-5)

Safety Data

• Hazardous Substances Data: 88016-17-5(Hazardous Substances Data)

Usage

General Description

2-Pyrrolidinone,4-amino-(9CI) is a chemical compound with the molecular formula C4H8N2O. It is also known by its systematic name 4-oxo-1-pyrrolidine-1-amine. 2-Pyrrolidinone,4-amino-(9CI) is a derivative of 2-Pyrrolidinone and is used in various industrial applications, including as a precursor in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is a white crystalline solid that is soluble in water and organic solvents. 2-Pyrrolidinone,4-amino-(9CI) has the potential to be a valuable building block in organic synthesis due to its reactivity and versatility in forming diverse chemical products. Its properties and applications make it an important compound in the field of organic chemistry and chemical manufacturing.

Upstream product

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Relevant articles and documents

PYRROLIDINE DERIVATIVES WITH ANTIBACTERIAL PROPERTIES

Provided is a compound of Formula (I) or a salt thereof: Formula (I) wherein R, m, n, R1, R2, Aa-Ac are defined as in the claims and ArI represents a bicyclic heterocyclic group of the following formula: Formula (2) Ar 2 represents a bicyclic heterocyclic group of the formula: [Formula 3] having antibacterial activity.

Synthesis of (R)-3,4-diaminobutanoic acid by desymmetrization of dimethyl 3-(benzylamino)glutarate through enzymatic ammonolysis

Lipase B from Candida antarctica is shown to be a highly efficient catalyst for the desymmetrization of dimethyl 3-(benzylamino)glutarate (1) through aminolysis and ammonolysis reactions. Using this procedure, enantiopure monoamides are obtained in high yield. The synthetic value of these compounds is demonstrated by the preparation of an enantiopure nonnatural amino acid, i.e. (R)-3,4-diaminobutanoic acid [(+)-12].