2-Pyrrolidinone, 4-(hydroxymethyl)-1-(phenylmethyl)-


Chemical Name: 2-Pyrrolidinone, 4-(hydroxymethyl)-1-(phenylmethyl)-
CAS Number: 96449-69-3
Product Number: AG00IJT9(AGN-PC-05XGHQ)
Synonyms:
MDL No: MFCD10003985
Molecular Formula: C12H15NO2
Molecular Weight: 205.2530

Identification/Properties


Computed Properties
Molecular Weight:
205.257g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
205.11g/mol
Monoisotopic Mass:
205.11g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
224
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-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



1-Benzyl-4-(hydroxymethyl)pyrrolidin-2-one, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique molecular structure allows for the introduction of functional groups at multiple positions, making it a valuable tool for organic chemists.In chemical synthesis, $name$ is often employed as a nucleophilic reagent in reactions such as acylation, alkylation, and condensation. Its hydroxymethyl group can undergo various transformations to introduce new chemical functionalities, enabling the synthesis of complex molecules with precise control over stereochemistry. Additionally, the benzyl moiety provides stability and protection to the molecule during synthetic processes.Furthermore, $name$ can participate in ring-forming reactions, leading to the formation of cyclic compounds with diverse applications. Its pyrrolidinone scaffold is particularly useful in the synthesis of heterocyclic compounds, which are prevalent in pharmaceuticals and agrochemicals.Overall, the versatile nature of 1-Benzyl-4-(hydroxymethyl)pyrrolidin-2-one makes it a valuable tool in organic synthesis, allowing chemists to access a wide range of structurally complex molecules with potential biological activities.