tert-butyl 8-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-1-carboxylate

95%

Reagent Code: #60430
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CAS Number 2246363-82-4

science Other reagents with same CAS 2246363-82-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 376.2538 g/mol
Formula C₁₉H₂₉BN₂O₅
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during reactions, making it suitable for multi-step synthetic processes. Its application is especially valuable in the development of biologically active compounds, where precise structural modifications are required.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿35,766.00
inventory 100mg
10-20 days ฿10,224.00

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tert-butyl 8-methyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine-1-carboxylate
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during reactions, making it suitable for multi-step synthetic processe

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it serves as a key intermediate. Its boronate ester group enables efficient participation in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals. The tert-butyloxycarbonyl (Boc) protecting group enhances its stability during reactions, making it suitable for multi-step synthetic processes. Its application is especially valuable in the development of biologically active compounds, where precise structural modifications are required.

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