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

96%

Reagent Code: #241717
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CAS Number 953411-16-0

science Other reagents with same CAS 953411-16-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.11 g/mol
Formula C₁₃H₁₈BN₃O₂
badge Registry Numbers
MDL Number MFCD16995867
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas from light

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active indazole derivatives. It plays an important role in pharmaceutical development, particularly in the construction of kinase inhibitors and anticancer agents. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry and drug discovery. Its amine functionality allows for further derivatization, enhancing its utility in creating diverse compound libraries for biological screening.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,060.00
inventory 250mg
10-20 days ฿1,820.00
inventory 1g
10-20 days ฿6,500.00
inventory 5g
10-20 days ฿32,340.00
inventory 10g
10-20 days ฿56,220.00

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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active indazole derivatives. It plays an important role in pharmaceutical development, particularly in the construction of kinase inhibitors and anticancer agents. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry and drug discovery. Its amine functionality allows for further derivatization, enhancing its utility in

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biologically active indazole derivatives. It plays an important role in pharmaceutical development, particularly in the construction of kinase inhibitors and anticancer agents. The boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry and drug discovery. Its amine functionality allows for further derivatization, enhancing its utility in creating diverse compound libraries for biological screening.

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