(5-(N-Cyclohexylsulfamoyl)-2-methoxyphenyl)boronic acid

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Reagent Code: #89342
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CAS Number 1704081-61-7

science Other reagents with same CAS 1704081-61-7

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Weight 313.18 g/mol
Formula C₁₃H₂₀BNO₅S
badge Registry Numbers
MDL Number MFCD28400437
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a cyclohexylsulfamoyl group and a methoxy substituent, enhances its stability and reactivity in these reactions. Additionally, it is employed in the development of bioactive compounds and as a building block in medicinal chemistry for designing potential drug candidates. Its utility in synthesizing complex organic molecules underscores its importance in research and industrial applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿42,100.00
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(5-(N-Cyclohexylsulfamoyl)-2-methoxyphenyl)boronic acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a cyclohexylsulfamoyl group and a methoxy substituent, enhances its stability and reactivity in these reactions. Additionally, it is employed in the development of bioactive compounds

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a cyclohexylsulfamoyl group and a methoxy substituent, enhances its stability and reactivity in these reactions. Additionally, it is employed in the development of bioactive compounds and as a building block in medicinal chemistry for designing potential drug candidates. Its utility in synthesizing complex organic molecules underscores its importance in research and industrial applications.

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