3-Pyrrolidinone


Chemical Name: 3-Pyrrolidinone
CAS Number: 96-42-4
Product Number: AG005ULH(AGN-PC-03R19F)
Synonyms:
MDL No:
Molecular Formula: C4H7NO
Molecular Weight: 85.1045

Identification/Properties


Properties
BP:
156 °C at 760 mmHg
Storage:
2-8℃;
Computed Properties
Molecular Weight:
85.106g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
85.053g/mol
Monoisotopic Mass:
85.053g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
69.9
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



3-Pyrrolidinone, also known as pyrrolidone, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, 3-Pyrrolidinone is commonly utilized as a building block in the synthesis of pharmaceuticals, agrochemicals, and various fine chemicals.Its cyclic structure and functional groups make 3-Pyrrolidinone an ideal starting material for the preparation of heterocyclic compounds and complex organic molecules. The presence of the pyrrolidine ring confers stability and conformational rigidity, making it a valuable scaffold for drug design and molecular modeling.In chemical synthesis, 3-Pyrrolidinone serves as a key intermediate in the construction of diverse chemical architectures. Its versatile nature allows for the introduction of different substituents and functional groups, enabling chemists to tailor the properties and reactivity of the final products.Furthermore, 3-Pyrrolidinone can participate in various organic reactions such as nucleophilic substitution, ring-opening reactions, and cycloadditions, offering synthetic chemists a wide array of strategies for building complex molecular structures.Overall, the application of 3-Pyrrolidinone in chemical synthesis plays a crucial role in the development of new pharmaceuticals, agrochemicals, and materials, showcasing its significance in the field of organic chemistry.