(1-(Methoxymethyl)-1H-pyrazol-4-yl)boronic acid

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Reagent Code: #202993
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CAS Number 1416785-98-2

science Other reagents with same CAS 1416785-98-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.95 g/mol
Formula C₅H₉BN₂O₃
badge Registry Numbers
MDL Number MFCD29761139
thermostat Physical Properties
Boiling Point 333.3±48.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.24±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole-containing compounds. Its primary application lies in pharmaceutical and agrochemical research, where it helps build biologically active molecules. The boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for creating diverse heterocyclic structures. It is particularly useful in developing kinase inhibitors and other therapeutic agents where the pyrazole scaffold is essential.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,770.00
inventory 1g
10-20 days ฿29,950.00

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(1-(Methoxymethyl)-1H-pyrazol-4-yl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole-containing compounds. Its primary application lies in pharmaceutical and agrochemical research, where it helps build biologically active molecules. The boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for creating diverse heterocyclic structures. It is particularly useful in developing kinase inhibitors and other therapeut

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex pyrazole-containing compounds. Its primary application lies in pharmaceutical and agrochemical research, where it helps build biologically active molecules. The boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for creating diverse heterocyclic structures. It is particularly useful in developing kinase inhibitors and other therapeutic agents where the pyrazole scaffold is essential.

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