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

95%

Reagent Code: #131924
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CAS Number 1256958-80-1

science Other reagents with same CAS 1256958-80-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.54 g/mol
Formula C₁₃H₁₇BClNO₃
badge Registry Numbers
MDL Number MFCD18383425
thermostat Physical Properties
Boiling Point 377.7±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.20±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. The amide functionality adds polarity and potential for hydrogen bonding, which can influence the reactivity and solubility in aqueous or polar organic solvents. Commonly employed in medicinal chemistry for constructing benzamide-based scaffolds with potential biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,300.00
inventory 1g
10-20 days ฿5,990.00
inventory 5g
10-20 days ฿20,950.00

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2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
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Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. The amide functionality adds polarity and potential for hydrogen bonding, which can influence the reactivity and solubility in aqueous or polar

Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive compounds and functional materials. The amide functionality adds polarity and potential for hydrogen bonding, which can influence the reactivity and solubility in aqueous or polar organic solvents. Commonly employed in medicinal chemistry for constructing benzamide-based scaffolds with potential biological activity.

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