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

98%

Reagent Code: #192712
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CAS Number 1613639-49-8

science Other reagents with same CAS 1613639-49-8

blur_circular Chemical Specifications

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Weight 278.54 g/mol
Formula C₁₃H₁₆BClN₂O₂
badge Registry Numbers
MDL Number MFCD16995865
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a key intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions to construct biaryl systems. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of active pharmaceutical ingredients (APIs) for oncology, CNS disorders, and inflammatory diseases. The indazole core is common in kinase inhibitors, and this compound facilitates the introduction of substituted indazole motifs into drug candidates. It is also employed in medicinal chemistry research for library synthesis in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,300.00
inventory 1g
10-20 days ฿45,000.00

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3-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
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Used primarily as a key intermediate in pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions to construct biaryl systems. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of active pharmaceutical ingredients (APIs) for oncology, CNS disorders, and inflammatory diseases. The indazole core is common in kinase inhibitors, and this compound facilitates the introduction of substituted indazole motifs into drug candidates. It is also employed in medicinal chemistry research for library synthesis in drug discovery programs.
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