3-(tert-butylamino)sulfonyl-phenylboronic acid pinacol ester

95%

Reagent Code: #242035
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CAS Number 706820-95-3

science Other reagents with same CAS 706820-95-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.26 g/mol
Formula C₁₆H₂₆BNO₄S
badge Registry Numbers
MDL Number MFCD18384175
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions. The tert-butylamino sulfonamide moiety enhances solubility and can act as a directing or stabilizing group in catalytic transformations. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,600.00
inventory 250mg
10-20 days ฿6,370.00
inventory 1g
10-20 days ฿16,360.00
inventory 5g
10-20 days ฿57,190.00

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3-(tert-butylamino)sulfonyl-phenylboronic acid pinacol ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions. The tert-butylamino sulfonamide moiety enhances solubility and can act as a directing or stabilizing group in catalytic transformations. Commonly employed in the development of bioactive compounds and functional materials where p

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient carbon-carbon bond formation under mild conditions. The tert-butylamino sulfonamide moiety enhances solubility and can act as a directing or stabilizing group in catalytic transformations. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required.

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