1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-1-yl)ethanone

97%

Reagent Code: #238209
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CAS Number 1158680-96-6

science Other reagents with same CAS 1158680-96-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.134 g/mol
Formula C₁₅H₁₉BN₂O₃
badge Registry Numbers
MDL Number MFCD24040116
thermostat Physical Properties
Melting Point 128 °C
Boiling Point 438.8±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in pharmaceutical synthesis, especially in the development of kinase inhibitors for cancer treatment. Its boron-containing group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing efficient formation of carbon-carbon bonds during the preparation of complex drug molecules. This compound is particularly valuable in medicinal chemistry for constructing indazole-based scaffolds, which are present in several bioactive molecules and investigational drugs targeting oncology and inflammatory diseases.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,290.00
inventory 1g
10-20 days ฿3,310.00
inventory 5g
10-20 days ฿11,530.00
1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-1-yl)ethanone
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Used primarily as an intermediate in pharmaceutical synthesis, especially in the development of kinase inhibitors for cancer treatment. Its boron-containing group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing efficient formation of carbon-carbon bonds during the preparation of complex drug molecules. This compound is particularly valuable in medicinal chemistry for constructing indazole-based scaffolds, which are present in several bioactive molecules and investigational drug

Used primarily as an intermediate in pharmaceutical synthesis, especially in the development of kinase inhibitors for cancer treatment. Its boron-containing group enables participation in Suzuki-Miyaura cross-coupling reactions, allowing efficient formation of carbon-carbon bonds during the preparation of complex drug molecules. This compound is particularly valuable in medicinal chemistry for constructing indazole-based scaffolds, which are present in several bioactive molecules and investigational drugs targeting oncology and inflammatory diseases.

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