2-Azetidinone, 4-phenyl-


Chemical Name: 2-Azetidinone, 4-phenyl-
CAS Number: 5661-55-2
Product Number: AG00EE31(AGN-PC-009I72)
Synonyms:
MDL No:
Molecular Formula: C9H9NO
Molecular Weight: 147.1739

Identification/Properties


Computed Properties
Molecular Weight:
147.177g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
147.068g/mol
Monoisotopic Mass:
147.068g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
161
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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
Precautionary Statements:
P261-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



4-Phenylazetidin-2-one is a versatile compound that finds extensive applications in chemical synthesis processes. As a cyclic amide, it serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. This molecule's unique structure allows for the introduction of diverse functional groups, enabling chemists to tailor its properties for specific applications.In chemical synthesis, 4-Phenylazetidin-2-one is commonly used as a key intermediate in the preparation of bioactive compounds and complex organic molecules. Its reactive nature allows for the formation of important carbon-carbon and carbon-nitrogen bonds, essential for constructing intricate molecular frameworks. Furthermore, its cyclic structure imparts rigidity and stereochemistry control in the final products, making it an ideal starting material for the synthesis of chiral compounds.Moreover, 4-Phenylazetidin-2-one can undergo various transformations, such as ring-opening reactions, functional group manipulations, and cyclization processes, making it a versatile tool in the hands of synthetic chemists. By leveraging its reactivity and structural features, researchers can access a wide range of chemical space and develop novel molecules with desired properties.Overall, the application of 4-Phenylazetidin-2-one in chemical synthesis offers a pathway to the efficient and controlled construction of diverse organic molecules with potential applications in pharmaceuticals, materials science, and other fields. Its utility lies in its ability to serve as a scaffold for molecular design and to facilitate the creation of complex, functionalized compounds with targeted properties.