3-Amino-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

95%

Reagent Code: #117764
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CAS Number 1036991-35-1

science Other reagents with same CAS 1036991-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.1 g/mol
Formula C₁₃H₁₇BN₂O₂
badge Registry Numbers
MDL Number MFCD22494384
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a valuable building block for creating complex organic molecules, especially in the pharmaceutical industry for developing drug candidates. The boronate ester group at the 5-position enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. The benzonitrile moiety at the 1-position and the amino group at the 3-position can be further modified, making it versatile for constructing diverse chemical structures with multiple functionalization sites. Its applications extend to material science, where it is used in the synthesis of advanced materials with potential electronic or optical properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,000.00
inventory 100mg
10-20 days ฿1,971.00
inventory 250mg
10-20 days ฿3,339.00

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3-Amino-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a valuable building block for creating complex organic molecules, especially in the pharmaceutical industry for developing drug candidates. The boronate ester group at the 5-position enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. The benzonitrile moiety at the 1-position and the amino group at the 3-position can

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a valuable building block for creating complex organic molecules, especially in the pharmaceutical industry for developing drug candidates. The boronate ester group at the 5-position enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. The benzonitrile moiety at the 1-position and the amino group at the 3-position can be further modified, making it versatile for constructing diverse chemical structures with multiple functionalization sites. Its applications extend to material science, where it is used in the synthesis of advanced materials with potential electronic or optical properties.

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