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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-(3-aminophenyl)pyrrolidin-2-one;hydrochloride

O=C1NCC(C1)c1cccc(c1)N.Cl Request for Quotation
Chemical Name: 4-(3-aminophenyl)pyrrolidin-2-one;hydrochloride
CAS Number: 1187830-88-1
Product Number: AG008TZV(AGN-PC-0BKEPJ)
Synonyms:
MDL No:
Molecular Formula: C10H13ClN2O
Molecular Weight: 212.6760

Identification/Properties

Computed Properties
Molecular Weight:
212.677g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
212.072g/mol
Monoisotopic Mass:
212.072g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
205
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(3-Aminophenyl)pyrrolidin-2-one hydrochloride is a versatile compound commonly utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceutical intermediates. In particular, it is frequently employed in the synthesis of drugs, agrochemicals, and fine chemicals.Due to the presence of the amino and pyrrolidinone groups in its structure, 4-(3-Aminophenyl)pyrrolidin-2-one hydrochloride can participate in a range of chemical reactions, such as nucleophilic substitution, acylation, and condensation reactions. These reactions allow for the introduction of functional groups and structural modifications, making it an indispensable tool in the creation of complex molecular structures.Additionally, the hydrochloride salt form of this compound provides enhanced solubility in aqueous solutions, making it easier to handle and manipulate in various synthetic processes. Its compatibility with a wide range of reaction conditions and its ability to facilitate the formation of key chemical bonds make it a valuable asset in the toolbox of synthetic chemists striving to develop novel compounds with diverse applications.