Cyclopentylboronic Acid (contains varying amounts of Anhydride)
≥97%
Reagent
Code: #91176
CAS Number
63076-51-7
blur_circular Chemical Specifications
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Molecular Information
Weight
113.95 g/mol
Formula
C₅H₁₁BO₂
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Registry Numbers
MDL Number
MFCD01074541
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Physical Properties
Melting Point
126°C dec. (Lit.)
Boiling Point
235 °C at 760 mmHg
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Storage & Handling
Density
1.03±0.1 g/cm3
Storage
2~8°C, sealed
description Product Description
Cyclopentylboronic acid, often containing varying amounts of its anhydride, is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its cyclopentyl group contributes to the steric and electronic properties of the resulting compounds, making it valuable in designing drugs and other bioactive molecules. Additionally, it serves as a key intermediate in the production of fine chemicals and functionalized organic compounds. The presence of the anhydride form can enhance reactivity in certain applications, offering versatility in synthetic pathways.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Purity | 96.5-100 |
Melting point | 124-128 |
Appearance | White to off-white, very pale yellow to pale reddish yellow, crystal to powder |
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Cyclopentylboronic Acid (contains varying amounts of Anhydride)
Cyclopentylboronic acid, often containing varying amounts of its anhydride, is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its cyclopentyl group contributes to the steric and electronic properties of the resulting compounds, making it valuable in designing drugs and other bioactive molecules. Additionally, it serves as a key intermediate in the production of fine chemicals and functionalized organic compounds. The presence of the anhydride form can enhance reactivity in certain applications, offering versatility in synthetic pathways.
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