5-Bromo-6-chloro-1H-indazole

95%

Reagent Code: #173681
fingerprint
CAS Number 1260382-77-1

science Other reagents with same CAS 1260382-77-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.48 g/mol
Formula C₇H₄BrClN₂
badge Registry Numbers
MDL Number MFCD18381158
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated indazole structure, which allows for selective cross-coupling reactions. Its derivatives are explored for anti-inflammatory, antiviral, and neuroprotective activities. Also employed in research settings to design and optimize new bioactive molecules targeting central nervous system disorders and oncology pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,230.00
inventory 5g
10-20 days ฿9,400.00
inventory 25g
10-20 days ฿40,790.00
inventory 10g
10-20 days ฿18,770.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Bromo-6-chloro-1H-indazole
No image available

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated indazole structure, which allows for selective cross-coupling reactions. Its derivatives are explored for anti-inflammatory, antiviral, and neuroprotective activities. Also employed in research settings to design and optimize new bioactive molecules targeting central nervous

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its halogenated indazole structure, which allows for selective cross-coupling reactions. Its derivatives are explored for anti-inflammatory, antiviral, and neuroprotective activities. Also employed in research settings to design and optimize new bioactive molecules targeting central nervous system disorders and oncology pathways.

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...