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CAS 15862-51-8

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5-Amino-3-bromo-1-methyl-2(1H)-pyridinone

Description:
5-Amino-3-bromo-1-methyl-2(1H)-pyridinone is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features an amino group (-NH2) and a bromo substituent (-Br) at specific positions on the pyridine ring, contributing to its reactivity and potential applications in various chemical reactions. The methyl group (-CH3) attached to the nitrogen enhances its lipophilicity, which can influence its biological activity and solubility in organic solvents. The presence of both the amino and bromo groups makes it a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Additionally, the compound's unique structure may impart specific properties such as antimicrobial or anti-inflammatory activities, making it of interest in medicinal chemistry. As with many nitrogen-containing heterocycles, it may also exhibit coordination chemistry with metal ions, further expanding its potential applications in materials science and catalysis.
Formula:C6H7BrN2O
InChI:InChI=1S/C6H7BrN2O/c1-9-3-4(8)2-5(7)6(9)10/h2-3H,8H2,1H3
InChI key:InChIKey=ACEXOLGEPCXWEB-UHFFFAOYSA-N
SMILES:O=C1C(Br)=CC(N)=CN1C
Synonyms:
  • 2(1H)-Pyridone, 5-amino-3-bromo-1-methyl-
  • 2(1H)-Pyridinone, 5-amino-3-bromo-1-methyl-
  • 5-Amino-3-bromo-1-methyl-2(1H)-pyridinone
  • 5-Amino-3-bromo-1-methyl-1H-pyridin-2-one
  • 5-amino-3-bromo-1-methyl-1,2-dihydropyridin-2-one
  • 5-Amino-3-bromo-1-methylpyridin-2(1H)-one
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