6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[4,3-a]pyridine

97%

Reagent Code: #241720
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CAS Number 1314137-24-0

science Other reagents with same CAS 1314137-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.09 g/mol
Formula C₁₂H₁₆BN₃O₂
badge Registry Numbers
MDL Number MFCD26403534
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl and heteroaryl frameworks. It is particularly useful in the development of kinase inhibitors and other bioactive molecules where the triazolopyridine scaffold enhances binding affinity and metabolic stability. The reagent’s compatibility with diverse functional groups allows for late-stage functionalization in complex molecule synthesis, streamlining drug discovery and optimization processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,760.00
inventory 250mg
10-20 days ฿6,150.00
inventory 1g
10-20 days ฿12,830.00
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-[1,2,4]triazolo[4,3-a]pyridine
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Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing biaryl and heteroaryl frameworks. It is particularly useful in the development of kinase inhibitors and other bioactive molecules where the triazolopyridine scaffold enhances binding affinity and metabolic stability. The reagent’s compatibility with diverse functional groups allows for late-stage functionalization in complex molecule synthesis, streamlining drug discovery and optimization processes.
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