7-Azaindole-3-boronic Acid Pinacol Ester

≥95%

Reagent Code: #90975
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CAS Number 945256-29-1

science Other reagents with same CAS 945256-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.10 g/mol
Formula C₁₃H₁₇N₂O₂B
badge Registry Numbers
MDL Number MFCD11616359
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of active pharmaceutical ingredients (APIs). Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable for synthesizing heterocyclic compounds, which are often found in drugs targeting various diseases. Additionally, it is employed in materials science for creating advanced organic materials with specific electronic or optical properties. 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 ฿6,264.00
inventory 1g
10-20 days ฿15,435.00

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7-Azaindole-3-boronic Acid Pinacol Ester
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of active pharmaceutical ingredients (APIs). Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable for synthesizing heterocyclic compounds, which are often foun

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical industry, where it aids in the development of active pharmaceutical ingredients (APIs). Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable for synthesizing heterocyclic compounds, which are often found in drugs targeting various diseases. Additionally, it is employed in materials science for creating advanced organic materials with specific electronic or optical properties. Its stability and reactivity make it a versatile tool in research and industrial applications.

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