5-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2H-tetrazole
95%
Reagent
Code: #90371
CAS Number
775351-40-1
blur_circular Chemical Specifications
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Molecular Information
Weight
272.11 g/mol
Formula
C₁₃H₁₇BN₄O₂
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Registry Numbers
MDL Number
MFCD12761127
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Physical Properties
Boiling Point
434.1±47.0 °C(Predicted)
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Storage & Handling
Density
1.22±0.1 g/cm3(Predicted)
Storage
2-8°C, sealed, dry
description Product Description
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of biaryl compounds, which are important in the development of pharmaceuticals, agrochemicals, and organic materials. The tetrazole moiety in the compound can act as a bioisostere for carboxylic acids, enhancing the biological activity of drug molecules. Additionally, the boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules. Its applications extend to materials science, where it is used in the development of polymers and advanced materials with specific electronic or optical properties.
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5-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-2H-tetrazole
This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the preparation of biaryl compounds, which are important in the development of pharmaceuticals, agrochemicals, and organic materials. The tetrazole moiety in the compound can act as a bioisostere for carboxylic acids, enhancing the biological activity of drug molecules. Additionally, the boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules. Its applications extend to materials science, where it is used in the development of polymers and advanced materials with specific electronic or optical properties.
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