tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate
≥95%
Reagent
Code: #114624
CAS Number
864771-44-8
blur_circular Chemical Specifications
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Molecular Information
Weight
344.21 g/mol
Formula
C₁₈H₂₅BN₂O₄
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Registry Numbers
MDL Number
MFCD08437629
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Physical Properties
Boiling Point
461.4°C at 760 mmHg
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Storage & Handling
Density
1.13g/cm3
Storage
2-8°C, store under inert gas
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of indazole derivatives, which are important scaffolds in drug discovery due to their biological activity. The tert-butyl group enhances stability and solubility, facilitating handling and reactivity in various synthetic processes. Additionally, it is used in the preparation of bioactive compounds, including potential therapeutic agents targeting cancer, inflammation, and other diseases. Its role in creating carbon-carbon bonds is crucial for developing novel organic materials and fine chemicals.
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tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, especially in pharmaceutical research and development. It is often employed in the synthesis of indazole derivatives, which are important scaffolds in drug discovery due to their biological activity. The tert-butyl group enhances stability and solubility, facilitating handling and reactivity in various synthetic processes. Additionally, it is used in the preparation of bioactive compounds, including potential therapeutic agents targeting cancer, inflammation, and other diseases. Its role in creating carbon-carbon bonds is crucial for developing novel organic materials and fine chemicals.
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