1,6-Dimethyl-1h-indazole

95%

Reagent Code: #177172
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CAS Number 34879-87-3

science Other reagents with same CAS 34879-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 146.19 g/mol
Formula C₉H₁₀N₂
badge Registry Numbers
MDL Number MFCD22380263
thermostat Physical Properties
Boiling Point 252.4±9.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.09±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily in research settings as a synthetic intermediate for developing pharmaceutical compounds. It serves as a building block in the synthesis of bioactive molecules, particularly in the design of kinase inhibitors and anti-inflammatory agents. Its structure is of interest in medicinal chemistry due to its similarity to purine bases, enabling potential interaction with enzyme active sites. Also explored in the development of novel psychoactive substances, though not approved for clinical or therapeutic use. Strictly for laboratory and analytical applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,900.00
inventory 250mg
10-20 days ฿31,180.00
inventory 1g
10-20 days ฿62,370.00

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1,6-Dimethyl-1h-indazole
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Used primarily in research settings as a synthetic intermediate for developing pharmaceutical compounds. It serves as a building block in the synthesis of bioactive molecules, particularly in the design of kinase inhibitors and anti-inflammatory agents. Its structure is of interest in medicinal chemistry due to its similarity to purine bases, enabling potential interaction with enzyme active sites. Also explored in the development of novel psychoactive substances, though not approved for clinical or therape
Used primarily in research settings as a synthetic intermediate for developing pharmaceutical compounds. It serves as a building block in the synthesis of bioactive molecules, particularly in the design of kinase inhibitors and anti-inflammatory agents. Its structure is of interest in medicinal chemistry due to its similarity to purine bases, enabling potential interaction with enzyme active sites. Also explored in the development of novel psychoactive substances, though not approved for clinical or therapeutic use. Strictly for laboratory and analytical applications.
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