4128-00-1

Basic information

• Product Name: (S)-3-AMINO-2-PYRROLIDINONE
• Synonyms: (S)-3-AMINO-2-PYRROLIDINONE;(S)-3-aMinopyrrolidin-2-one;(3S)-3-aMinopyrrolidin-2-one;(S)-3-AMINO-2-PYRROLIDINONE hcl;(3S)-3-Amino-2-pyrrolidinone;L-3-Amino-2-pyrrolidone;L-3-Amino-pyrrolidinone
• CAS NO: 4128-00-1
• Molecular Formula: C₄H₈N₂O
• Molecular Weight: 100.1191
• Mol File: 4128-00-1.mol
• Article Data: 8

Chemical Properties

• Melting Point: 120-130℃
• Boiling Point: 306℃
• Flash Point: 139℃
• Appearance: /
• Density: 1.127
• Storage Temp.: 2-8°C(protect from light)
• PKA: 15.92±0.40(Predicted)
• CAS DataBase Reference: (S)-3-AMINO-2-PYRROLIDINONE(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-3-AMINO-2-PYRROLIDINONE(4128-00-1)
• EPA Substance Registry System: (S)-3-AMINO-2-PYRROLIDINONE(4128-00-1)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45
• Hazardous Substances Data: 4128-00-1(Hazardous Substances Data)

Usage

General Description

(S)-3-Amino-2-pyrrolidinone is a chemical compound that falls under the category of pyrrolidinones, a subclass of pyrrolidines. The compound is recognized by the formula C4H8N2O, and it primarily exists as a solid at room temperature. It is a chiral compound, and this particular version represents the S-isomer. The primary application of this compound is in the field of organic synthesis, where it can serve as an enantiomerically pure building block for the synthesis of more complex molecules. Its potential toxicity or health effects have not been extensively studied, making it crucial for those handling it to take necessary precautions.

Upstream product

• 141-52-6 sodium ethanolate 
• 103668-08-2 ethyl (S)-2,4-diaminobutanoate dihydrochloride 
• 1758-80-1 L-2,4-diaminobutyrate 
• 1482-98-0 L-2,4-diaminobutyric acid monohydrochloride 
• 1482-98-0 (S)-2,4-diaminobutyric acid dihydrochloride 

Downstream Products

• 146679-04-1 (S)-3-(formylamino)-2-pyrrolidinone 
• 114200-45-2 3(S)-amino>-2-oxopyrrolidine 

Relevant articles and documents

ACC INHIBITORS AND USES THEREOF

The present invention provides compounds I and II useful as inhibitors of Acetyl CoA Carboxylase (ACC), compositions thereof, and methods of using the same.

Kinase inhibitor compounds

The invention relates to compounds, compositions comprising the compounds, and methods of using the compounds and compound compositions. The compounds, compositions, and methods described herein can be used for the therapeutic modulation of kinase-mediated processes, and treatment of disease and disease symptoms, particularly those mediated by certain kinase enzymes.

P38 INHIBITORS AND METHODS OF USE THEREOF

Compounds of formula (I): in which A, B, X, Ar1, R8 and R4 have any of the meanings given in the specification, are inhibitors of p38 useful in the treatment and prevention of various disorders mediated by p38.