1-(pyridin-2-yl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea

97%

Reagent Code: #223314
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CAS Number 874297-97-9

science Other reagents with same CAS 874297-97-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 339.1966 g/mol
Formula C₁₈H₂₂BN₃O₃
thermostat Physical Properties
Boiling Point 415.6±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.18±0.1 g/cm3(Predicted)
Storage 2-8°C

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 the development of complex organic molecules, particularly in drug discovery and materials science. The urea linkage also allows for hydrogen bonding, which can be exploited in the design of functional materials or bioactive compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿16,000.00
250mg
10-20 days ฿32,000.00
1g
10-20 days ฿67,200.00
1-(pyridin-2-yl)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)urea
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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 the development of complex organic molecules, particularly in drug discovery and materials science. The urea linkage also allows for hydrogen bonding, which can be exploited in the design of functional materials or bioactive compounds.

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 the development of complex organic molecules, particularly in drug discovery and materials science. The urea linkage also allows for hydrogen bonding, which can be exploited in the design of functional materials or bioactive compounds.

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