CAS 79173-62-9
:3-methyl-1H-indazol-6-amine
Description:
3-Methyl-1H-indazol-6-amine is an organic compound characterized by its indazole core, which consists of a five-membered ring fused to a six-membered aromatic ring. The presence of a methyl group at the 3-position and an amino group at the 6-position contributes to its unique chemical properties. This compound typically appears as a solid and is soluble in polar organic solvents. It is of interest in medicinal chemistry due to its potential biological activities, including anti-cancer and anti-inflammatory properties. The amino group can participate in hydrogen bonding, influencing its reactivity and interactions with biological targets. Additionally, the compound may exhibit various functional properties, such as being a potential ligand in coordination chemistry or a precursor in organic synthesis. Safety and handling precautions should be observed, as with many organic compounds, due to potential toxicity or reactivity. Overall, 3-methyl-1H-indazol-6-amine is a versatile compound with applications in research and development within the pharmaceutical industry.
Formula:C8H9N3
InChI:InChI=1/C8H9N3/c1-5-7-3-2-6(9)4-8(7)11-10-5/h2-4H,9H2,1H3,(H,10,11)
SMILES:Cc1c2ccc(cc2n[nH]1)N
Synonyms:- 1H-Indazol-6-aMine,3-Methyl-
- CC1=NNC2=C1C=CC(N)=C2
- Pazopanib Impurity 58
- 6-AMINO-3-MRTHYL(1H)INDAZOLE
- 3-methyl-1H-indazol-6-amine
- 3-Methyl-1H-indazol-6-ylamine ,97%
- 6-Amino-3-methylindazole
- 6-AMino-3-Methyl (1H)indazole
- 3-Methyl-1H-indazol-6-ylamine
- 3-Methyl-2H-indazol-6-aMine
- See more synonyms
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Found 5 products.
3-Methyl-1H-indazol-6-amine
CAS:Formula:C8H9N3Purity:97%Color and Shape:SolidMolecular weight:147.17723-Methyl-1H-indazol-6-ylamine
CAS:Formula:C8H9N3Purity:98%Color and Shape:SolidMolecular weight:147.1813-Methyl-1H-indazol-6-amine
CAS:<p>3-Methyl-1H-indazol-6-amine is an organic compound that belongs to the group of diazo compounds. It is a benzene derivative with three alkoxy groups, which are substituted with an alkyl or an aryl group. 3-Methyl-1H-indazol-6-amine can be synthesized by coupling the corresponding chlorides with toluene and diazonium salts in an alkaline solution. The fibre used for this synthesis has been shown to have aryl and alkyl groups. This compound reacts with acid as hydrogen chloride, resulting in the release of carbon dioxide gas. 3-Methyl-1H-indazol-6-amine also reacts readily with water and alcohols, forming indazole hydrochloride and benzoic acid respectively.</p>Formula:C8H9N3Purity:Min. 95%Molecular weight:147.18 g/mol



