2-(6-Bromo-1H-indazol-3-yl)acetic acid

95%

Reagent Code: #149370
fingerprint
CAS Number 944904-66-9

science Other reagents with same CAS 944904-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.07 g/mol
Formula C₉H₇BrN₂O₂
badge Registry Numbers
MDL Number MFCD09835480
thermostat Physical Properties
Boiling Point 484.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in pharmaceutical research as a key intermediate for synthesizing biologically active compounds, particularly kinase inhibitors. Shows relevance in developing anticancer agents due to its structural similarity to indazole-based inhibitors that target signaling pathways in tumor cells. Also employed in the synthesis of analogs for structure-activity relationship (SAR) studies, helping optimize potency and selectivity in drug candidates. Its carboxylic acid group allows for easy derivatization, making it valuable in medicinal chemistry for amide coupling and prodrug formation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,540.00
inventory 250mg
10-20 days ฿18,960.00
inventory 1g
10-20 days ฿47,330.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(6-Bromo-1H-indazol-3-yl)acetic acid
No image available

Used in pharmaceutical research as a key intermediate for synthesizing biologically active compounds, particularly kinase inhibitors. Shows relevance in developing anticancer agents due to its structural similarity to indazole-based inhibitors that target signaling pathways in tumor cells. Also employed in the synthesis of analogs for structure-activity relationship (SAR) studies, helping optimize potency and selectivity in drug candidates. Its carboxylic acid group allows for easy derivatization, making

Used in pharmaceutical research as a key intermediate for synthesizing biologically active compounds, particularly kinase inhibitors. Shows relevance in developing anticancer agents due to its structural similarity to indazole-based inhibitors that target signaling pathways in tumor cells. Also employed in the synthesis of analogs for structure-activity relationship (SAR) studies, helping optimize potency and selectivity in drug candidates. Its carboxylic acid group allows for easy derivatization, making it valuable in medicinal chemistry for amide coupling and prodrug formation.

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...