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

97%

Reagent Code: #131017
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CAS Number 957346-54-2

science Other reagents with same CAS 957346-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.09 g/mol
Formula C₁₃H₁₇BFNO₃
badge Registry Numbers
MDL Number MFCD18732743
thermostat Physical Properties
Boiling Point 358.2±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for building complex aromatic structures. The presence of a fluorine atom enhances binding selectivity and metabolic stability in target molecules. Commonly employed in the development of kinase inhibitors and other bioactive compounds where fluorinated aromatic scaffolds are required.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,380.00
1g
10-20 days ฿9,030.00
3-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for building complex aromatic structures. The presence of a fluorine atom enhances binding selectivity and metabolic stability in target molecules. Commonly employed in the development of kinase inhibitors and other bioactiv

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for building complex aromatic structures. The presence of a fluorine atom enhances binding selectivity and metabolic stability in target molecules. Commonly employed in the development of kinase inhibitors and other bioactive compounds where fluorinated aromatic scaffolds are required.

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