1-(1-methyl-1H-indazol-7-yl)ethanone

1-(1-methyl-1H-indazol-7-yl)ethanone

4-bromo-3-chloro-1H-indazole

4-bromo-3-chloro-1H-indazole

1-methyl-1H-indazol-7-amine

$300.00
CAS No.: 41926-06-1
Catalog No.: 196195
Purity: 95%
MF: C8H9N3
MW: 147.181
Storage: 2-8 degree Celsius
SMILES: CN1N=CC2=CC=CC(=C12)N
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196195
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1-methyl-1H-indazol-7-amine; CAS No.: 41926-06-1; 1-methyl-1H-indazol-7-amine. PROPERTIES: This compound features a 1-methyl-1H-indazol-7-amine structure, combining an amino group and a methyl-substituted indazole ring system. It typically appears as a white to off-white crystalline solid with a molecular weight of approximately 170.2 g/mol (C10H10N4). The melting point ranges between 120-125 C, and it exhibits moderate solubility in common organic solvents like ethanol, methanol, and DMSO while being sparingly soluble in water. Proper storage requires a tightly sealed container in a cool, dry place. Safety precautions include wearing appropriate PPE. It is classified as a skin and eye irritant (GHS07) with the hazard statement H315-H319. APPLICATIONS: 1-Methyl-1H-indazol-7-amine serves as a valuable intermediate in pharmaceutical and chemical synthesis. Its 1-methyl-1H-indazol-7-amine structure enables diverse reactivity patterns, including acylation, sulfonation, and coupling reactions at the amino group. In medicinal chemistry, it is used to develop bioactive molecules targeting the central nervous system and inflammatory pathways. The amino group can be modified to introduce various pharmacophoric elements. This compound also functions as a building block in the synthesis of fluorescent dyes and bioconjugation reagents. Academic studies employ it as a model compound in Medicinal Chemistry journals, focusing on the development of novel indazole derivatives based on the 1-methyl-1H-indazol-7-amine scaffold.

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