2H-Pyrrol-2-one, 1,5-dihydro-4-methoxy-


Chemical Name: 2H-Pyrrol-2-one, 1,5-dihydro-4-methoxy-
CAS Number: 69778-83-2
Product Number: AG003LMY(AGN-PC-0JT53O)
Synonyms:
MDL No:
Molecular Formula: C5H7NO2
Molecular Weight: 113.1146

Identification/Properties


Properties
MP:
129-132 °C(lit.)
BP:
349.6 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
113.116g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
113.048g/mol
Monoisotopic Mass:
113.048g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
139
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



1,5-Dihydro-4-methoxy-2H-pyrrol-2-one is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 1,5-Dihydro-4-methoxy-2H-pyrrol-2-one acts as a valuable intermediate in many organic reactions. Its cyclic structure and functional groups provide opportunities for diverse transformations, such as ring-opening reactions, nucleophilic additions, and substitution reactions. This compound can be leveraged to introduce specific functional groups into a molecule, alter stereochemistry, or form complex ring systems.Moreover, the methoxy substituent on the pyrrole ring enhances the electron density in the molecule, making it a useful nucleophile or a directing group in transition metal-catalyzed reactions. This can facilitate the selective formation of desired products in synthetic pathways.Overall, the strategic incorporation of 1,5-Dihydro-4-methoxy-2H-pyrrol-2-one in chemical synthesis enables chemists to access a wide array of structurally diverse compounds with potential applications in drug discovery, material science, and other fields requiring tailored molecules.