1-(3-aminophenyl)imidazolidin-2-one


Chemical Name: 1-(3-aminophenyl)imidazolidin-2-one
CAS Number: 938459-14-4
Product Number: AG00GVMQ(AGN-PC-04PBPN)
Synonyms:
MDL No:
Molecular Formula: C9H11N3O
Molecular Weight: 177.2031

Identification/Properties


Computed Properties
Molecular Weight:
177.207g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
177.09g/mol
Monoisotopic Mass:
177.09g/mol
Topological Polar Surface Area:
58.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
207
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-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



1-(3-Aminophenyl)imidazolidin-2-one, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties. This compound is especially valued for its ability to act as a versatile building block in the creation of various organic molecules. Its distinct structure containing an aminophenyl group and an imidazolidin-2-one ring provides a diverse range of functional groups for modification and manipulation in complex synthesis routes.In chemical synthesis, $name$ serves as a valuable intermediate in the production of pharmaceuticals, agrochemicals, and materials. Its presence allows for the introduction of specific functional groups, enabling the synthesis of compounds with desired biological activities or physical properties. Furthermore, the imidazolidin-2-one ring confers stability and rigidity to the molecule, making it a useful scaffold in the design of novel molecules with predefined three-dimensional structures.Moreover, the aminophenyl group in $name$ offers the opportunity for further derivatization through traditional organic transformations, such as acylation, alkylation, or cross-coupling reactions. This property enhances the versatility of the compound, enabling chemists to tailor its chemical structure for specific applications in synthetic chemistry.Overall, the application of 1-(3-Aminophenyl)imidazolidin-2-one in chemical synthesis showcases its significance as a valuable building block with diverse functionalization potential, making it indispensable for the creation of complex organic molecules with tailored properties.