(4-(tert-Butoxycarbonyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-7-yl)boronic acid

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Reagent Code: #113276
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CAS Number 2304633-98-3

science Other reagents with same CAS 2304633-98-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.1 g/mol
Formula C₁₃H₁₈BNO₅
badge Registry Numbers
MDL Number MFCD28061758
thermostat Physical Properties
Boiling Point 452.7±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.27±0.1 g/cm3(Predicted)
Storage 2-8°C, inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, its tert-butoxycarbonyl (Boc) protecting group enhances stability during synthetic processes, allowing for selective deprotection when needed. This compound is especially useful in medicinal chemistry for developing drug candidates with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,500.00

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(4-(tert-Butoxycarbonyl)-3,4-dihydro-2H-benzo[b][1,4]oxazin-7-yl)boronic acid
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, its tert-butoxycarbonyl (Boc) protecting group enhances stability during synthetic processes, allowing

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. Additionally, its tert-butoxycarbonyl (Boc) protecting group enhances stability during synthetic processes, allowing for selective deprotection when needed. This compound is especially useful in medicinal chemistry for developing drug candidates with improved efficacy and selectivity.

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