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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)-1H-pyridin-2-one;hydrochloride

NCc1cc[nH]c(=O)c1.Cl Request for Quotation
Chemical Name: 4-(aminomethyl)-1H-pyridin-2-one;hydrochloride
CAS Number: 943751-21-1
Product Number: AG006BD4(AGN-PC-0BSYVF)
Synonyms:
MDL No:
Molecular Formula: C6H9ClN2O
Molecular Weight: 160.6015

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
160.601g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
160.04g/mol
Monoisotopic Mass:
160.04g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
182
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Aminomethyl)pyridin-2(1H)-one hydrochloride is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals due to its multi-functional nature.In chemical synthesis, 4-(Aminomethyl)pyridin-2(1H)-one hydrochloride acts as a key intermediate in the synthesis of complex organic compounds. Its amino and pyridine functionalities enable it to participate in a wide range of reactions, such as nucleophilic substitution, condensation, and cyclization reactions. These reactions allow for the formation of diverse chemical structures with tailored properties.Furthermore, the hydrochloride salt form of 4-(Aminomethyl)pyridin-2(1H)-one enhances its solubility in polar solvents, facilitating its use in aqueous reactions and purification processes. This characteristic makes it a preferred choice in the development of pharmaceutical compounds, where aqueous reaction conditions are often employed for safety and regulatory reasons.Overall, 4-(Aminomethyl)pyridin-2(1H)-one hydrochloride is a valuable tool in the hands of synthetic chemists, enabling the efficient construction of complex molecules with specific properties and functionalities. Its versatile reactivity and solubility characteristics make it an indispensable component in modern organic synthesis strategies.