3-Bromo-1H-indazole-5-carbonitrile

95%

Reagent Code: #148199
fingerprint
CAS Number 395101-67-4

science Other reagents with same CAS 395101-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.04 g/mol
Formula C₈H₄BrN₃
badge Registry Numbers
MDL Number MFCD09263218
thermostat Physical Properties
Boiling Point 425.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used 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 ability to undergo cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing bioactive molecules with potential anti-inflammatory, antiviral, and antitumor activities. Its nitrile and bromo functional groups allow for selective modifications, making it valuable in structure-activity relationship (SAR) studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,320.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Bromo-1H-indazole-5-carbonitrile
No image available

Used 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 ability to undergo cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing bioactive molecules with potential anti-inflammatory, antiviral, and antitumor activities. Its nitrile and bromo functional groups allow for

Used 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 ability to undergo cross-coupling reactions, enabling the construction of complex heterocyclic systems. Commonly employed in research settings for designing bioactive molecules with potential anti-inflammatory, antiviral, and antitumor activities. Its nitrile and bromo functional groups allow for selective modifications, making it valuable in structure-activity relationship (SAR) studies.

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...