3-Bromo-1H-indazole-7-carboxylic acid

95%

Reagent Code: #146749
fingerprint
CAS Number 1040101-01-6

science Other reagents with same CAS 1040101-01-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.04 g/mol
Formula C₈H₅BrN₂O₂
thermostat Physical Properties
Boiling Point 493.4°C
inventory_2 Storage & Handling
Storage 2-8°C

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 form substituted indazole derivatives, which are present in various biologically active molecules. Its carboxylic acid and bromo functional groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also employed in the preparation of agrochemicals and in research involving heterocyclic compounds with potential anti-inflammatory or antimicrobial properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿291.50
inventory 250mg
10-20 days ฿891.00
inventory 5g
10-20 days ฿16,740.00
inventory 1g
10-20 days ฿1,914.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Bromo-1H-indazole-7-carboxylic acid
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 form substituted indazole derivatives, which are present in various biologically active molecules. Its carboxylic acid and bromo functional groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also employed in the prep

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 form substituted indazole derivatives, which are present in various biologically active molecules. Its carboxylic acid and bromo functional groups allow for further chemical modifications, enabling the creation of diverse compound libraries for drug discovery. Also employed in the preparation of agrochemicals and in research involving heterocyclic compounds with potential anti-inflammatory or antimicrobial properties.

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...