(4-(N-Cyclopentylsulfamoyl)-3, 5-dimethylphenyl)boronic acid

98%

Reagent Code: #89269
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CAS Number 1704097-46-0

science Other reagents with same CAS 1704097-46-0

blur_circular Chemical Specifications

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Weight 297.18 g/mol
Formula C₁₃H₂₀BNO₄S
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It acts as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structure, featuring a cyclopentylsulfamoyl group, may contribute to enhanced stability or selectivity in certain reactions. Additionally, it can be employed in the development of bioactive compounds or as an intermediate in the preparation of advanced materials. Its application is often tailored to specific research or industrial needs, particularly in fields requiring precise molecular construction.

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inventory 1g
10-20 days ฿44,770.00
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(4-(N-Cyclopentylsulfamoyl)-3, 5-dimethylphenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It acts as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structure, featuring a cyclopentylsulfamoyl group, may contribute to enhanced stability or selectivity in certain reactions. Additionally, it can be employed in the development of

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It acts as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structure, featuring a cyclopentylsulfamoyl group, may contribute to enhanced stability or selectivity in certain reactions. Additionally, it can be employed in the development of bioactive compounds or as an intermediate in the preparation of advanced materials. Its application is often tailored to specific research or industrial needs, particularly in fields requiring precise molecular construction.

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