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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-(Aminomethyl)-1-methylpyrrolidin-2-one

NCC1CC(=O)N(C1)C Request for Quotation
Chemical Name: 4-(Aminomethyl)-1-methylpyrrolidin-2-one
CAS Number: 933723-27-4
Product Number: AG00GVT6(AGN-PC-0WB39U)
Synonyms:
MDL No:
Molecular Formula: C6H12N2O
Molecular Weight: 128.1723

Identification/Properties

Computed Properties
Molecular Weight:
128.175g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
128.095g/mol
Monoisotopic Mass:
128.095g/mol
Topological Polar Surface Area:
46.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
124
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#:
N/A
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Aminomethyl)-1-methylpyrrolidin-2-one is a versatile compound that finds widespread application in chemical synthesis. Due to its unique structure, this compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, it can be used as a key intermediate for the synthesis of diverse nitrogen-containing compounds. Its functional groups allow for easy modification, enabling chemists to tailor its structure for specific applications. Additionally, the presence of the amino group makes it a crucial precursor for the preparation of heterocyclic compounds. This compound's reactivity and flexibility make it an indispensable tool for chemists seeking to design and develop new molecules with enhanced properties.