7-Bromo-2,3-dimethyl-2H-indazole

98%

Reagent Code: #150429
fingerprint
CAS Number 845751-62-4

science Other reagents with same CAS 845751-62-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.09 g/mol
Formula C₉H₉BrN₂
badge Registry Numbers
MDL Number MFCD12028640
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure serves as a scaffold for compounds targeting inflammatory diseases, cancer, and neurological disorders. The bromo functional group allows for further modification via cross-coupling reactions, enabling rapid diversification in drug discovery programs. It is also employed in the synthesis of selective probes for studying enzyme activity and receptor binding.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,520.00
inventory 250mg
10-20 days ฿4,200.00
inventory 1g
10-20 days ฿10,970.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
7-Bromo-2,3-dimethyl-2H-indazole
No image available

Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure serves as a scaffold for compounds targeting inflammatory diseases, cancer, and neurological disorders. The bromo functional group allows for further modification via cross-coupling reactions, enabling rapid diversification in drug discovery programs. It is also employed in the synthesis of selective probes for studying enzyme activity an

Used primarily as a synthetic intermediate in pharmaceutical research, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure serves as a scaffold for compounds targeting inflammatory diseases, cancer, and neurological disorders. The bromo functional group allows for further modification via cross-coupling reactions, enabling rapid diversification in drug discovery programs. It is also employed in the synthesis of selective probes for studying enzyme activity and receptor binding.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...