7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinazoline

≥95%

Reagent Code: #120949
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CAS Number 1375108-46-5

science Other reagents with same CAS 1375108-46-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.11 g/mol
Formula C₁₄H₁₇BN₂O₂
badge Registry Numbers
MDL Number MFCD18205965
thermostat Physical Properties
Boiling Point 390.5±15.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronate ester group in the structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of quinazoline derivatives. These derivatives are often explored for their potential biological activities, including anticancer, antiviral, and anti-inflammatory properties. Additionally, it is utilized in materials science for the development of organic electronic materials and polymers. Its stability and reactivity make it a versatile tool in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,519.00
inventory 1g
10-20 days ฿31,284.00
inventory 100mg
10-20 days ฿7,857.00

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7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinazoline
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronate ester group in the structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of quinazoline derivatives. These derivatives are often explored for their potential biological activities, including anticance

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. The boronate ester group in the structure makes it a valuable reagent for forming carbon-carbon bonds, enabling the construction of quinazoline derivatives. These derivatives are often explored for their potential biological activities, including anticancer, antiviral, and anti-inflammatory properties. Additionally, it is utilized in materials science for the development of organic electronic materials and polymers. Its stability and reactivity make it a versatile tool in research and industrial applications.

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