8-(TEtramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-2H-1,4-benzoxazine

95%

Reagent Code: #243003
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CAS Number 2377610-89-2

science Other reagents with same CAS 2377610-89-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.13 g/mol
Formula C₁₄H₂₀BNO₃
badge Registry Numbers
MDL Number MFCD27936554
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as a key intermediate in pharmaceutical synthesis, this compound enables the formation of complex heterocyclic structures through Suzuki-Miyaura cross-coupling reactions. Its boron-containing group facilitates carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive molecules and drug candidates. It is especially useful in constructing benzoxazine-based scaffolds found in central nervous system agents and anti-inflammatory compounds. The reagent’s stability and reactivity profile allow for high selectivity and yield in late-stage functionalization of drug-like molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,220.00
inventory 250mg
10-20 days ฿22,780.00

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8-(TEtramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-2H-1,4-benzoxazine
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Used primarily as a key intermediate in pharmaceutical synthesis, this compound enables the formation of complex heterocyclic structures through Suzuki-Miyaura cross-coupling reactions. Its boron-containing group facilitates carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive molecules and drug candidates. It is especially useful in constructing benzoxazine-based scaffolds found in central nervous system agents and anti-inflammatory compounds. The reagen

Used primarily as a key intermediate in pharmaceutical synthesis, this compound enables the formation of complex heterocyclic structures through Suzuki-Miyaura cross-coupling reactions. Its boron-containing group facilitates carbon-carbon bond formation under mild conditions, making it valuable in the development of bioactive molecules and drug candidates. It is especially useful in constructing benzoxazine-based scaffolds found in central nervous system agents and anti-inflammatory compounds. The reagent’s stability and reactivity profile allow for high selectivity and yield in late-stage functionalization of drug-like molecules.

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