3-methyl-1H-indazol-6-amine Chemical Properties

Boiling point:

376.4±22.0 °C(Predicted)

Density 

1.295±0.06 g/cm3(Predicted)

storage temp. 

Keep in dark place,Inert atmosphere,Room temperature

pka

16.00±0.40(Predicted)

Safety Information

Risk Statements 

22-36/37/38

Safety Statements 

22-26-36/37/39

HS Code 

29339900

3-methyl-1H-indazol-6-amine Usage And Synthesis

Description

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.

Chemical Properties

Light yellow to brown solid

3-methyl-1H-indazol-6-amine(79173-62-9)Related Product Information

• 3-Methyl-6-nitroindazole
• 2-Ethyl-5-nitrobenzenamine ,98%
• 5-Amino-2-methylbenzenesulfonamide
• N4-(2,3-Dimethyl-2H-indazol-6-yl)-N4-methyl-2,4-pyrimidinediamine
• Pazopanib Impurity 48
• 5-Amino-2,3-dimethyl-2H-indazole
• Pazopanib Impurity 32
• 2,4-Dichloropyrimidine
• Benzenamine, 2-ethyl-4-nitro-
• 3-AMINO-4-METHYLBENZENESULFONAMIDE
• 2-amino-5-methylbenzenesulfonamide
• Pazopanib-d6
• 2H-Indazol-4-amine, 2,3-dimethyl-
• 1H-Indazol-6-amine, N-(2-chloro-4-pyrimidinyl)-3-methyl-
• 6-Nitroindazole
• Pazopanib Impurity 47
• 6-Nitro-3-indazolecarboxylic acid
• 6-Aminoindazole