Ethyl 6-bromo-1H-indazole-3-carboxylate

≥95%

Reagent Code: #181938
fingerprint
CAS Number 885272-94-6

science Other reagents with same CAS 885272-94-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.10 g/mol
Formula C₁₀H₉BrN₂O₂
badge Registry Numbers
MDL Number MFCD05664002
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of bioactive molecules, especially in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its bromo and ester functionalities allow for further chemical modifications, enabling the introduction of various substituents through cross-coupling reactions or hydrolysis. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the indazole core’s metabolic stability and resemblance to purine bases. Also utilized in the development of selective ligands for cannabinoid receptors in neuroscience research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿6,350.00
inventory 5g
10-20 days ฿31,680.00
inventory 10g
10-20 days ฿59,140.00
inventory 250mg
10-20 days ฿1,970.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 6-bromo-1H-indazole-3-carboxylate
No image available

Used primarily as a key intermediate in the synthesis of bioactive molecules, especially in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its bromo and ester functionalities allow for further chemical modifications, enabling the introduction of various substituents through cross-coupling reactions or hydrolysis. Commonly employed in medicinal chemistry for structure-activity relationship stu

Used primarily as a key intermediate in the synthesis of bioactive molecules, especially in pharmaceutical research. It serves as a building block for developing kinase inhibitors and other therapeutic agents targeting cancer and inflammatory diseases. Its bromo and ester functionalities allow for further chemical modifications, enabling the introduction of various substituents through cross-coupling reactions or hydrolysis. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the indazole core’s metabolic stability and resemblance to purine bases. Also utilized in the development of selective ligands for cannabinoid receptors in neuroscience research.

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...