tert-Butyl 2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate

95%

Reagent Code: #115508
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CAS Number 1005397-65-8

science Other reagents with same CAS 1005397-65-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.26 g/mol
Formula C₁₈H₃₂BNO₄
badge Registry Numbers
MDL Number MFCD14582863
thermostat Physical Properties
Boiling Point 368.8±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.03±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s structure, featuring a protected amine group, allows for selective functionalization, enabling the construction of diverse heterocyclic frameworks. Its stability and reactivity make it a preferred intermediate in medicinal chemistry for developing drug candidates. Additionally, it is employed in the preparation of boron-containing compounds, which are increasingly important in materials science and catalysis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,220.00
inventory 50mg
10-20 days ฿8,541.00
inventory 100mg
10-20 days ฿13,662.00

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tert-Butyl 2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate
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This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s structure, featuring a protected amine group, allows for selective functionalization, enabling the

This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s structure, featuring a protected amine group, allows for selective functionalization, enabling the construction of diverse heterocyclic frameworks. Its stability and reactivity make it a preferred intermediate in medicinal chemistry for developing drug candidates. Additionally, it is employed in the preparation of boron-containing compounds, which are increasingly important in materials science and catalysis.

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