2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole

≥95%

Reagent Code: #193955
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CAS Number 1189746-27-7

science Other reagents with same CAS 1189746-27-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.12 g/mol
Formula C₁₄H₁₉BN₂O₂
badge Registry Numbers
MDL Number MFCD11109436
thermostat Physical Properties
Boiling Point 404.4±18.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing complex indazole-based structures, which are common in bioactive molecules and drug candidates. Due to its stability and reactivity, it is widely employed in medicinal chemistry for lead optimization and library synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,520.00
250mg
10-20 days ฿2,480.00
1g
10-20 days ฿7,100.00
5g
10-20 days ฿21,880.00
10g
10-20 days ฿43,730.00
2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-indazole
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Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is especially valuable in constructing complex indazole-based structures, which are common in bioactive molecules and drug candidates. Due to its stability and reactivity, it is widely employed in medicinal chemistry for lead optimization and library synthesis.
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