N-cyclopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

97%

Reagent Code: #44713
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CAS Number 1416367-02-6

science Other reagents with same CAS 1416367-02-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.21548 g/mol
Formula C₁₅H₂₂BNO₄S
inventory_2 Storage & Handling
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description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This enables the synthesis of biaryl compounds, which are essential in the development of drugs, herbicides, and other bioactive molecules. Additionally, its sulfonamide group can contribute to the compound's role in designing molecules with specific biological activities, such as enzyme inhibition or receptor modulation. Its stability and reactivity make it a versatile tool in medicinal chemistry and material science research.

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Test Parameter Specification
Appearance White Powder
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,134.00
inventory 100mg
10-20 days ฿6,075.00
inventory 1g
10-20 days ฿26,982.00

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N-cyclopropyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide
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This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This enables the synthesis of biaryl compounds, which are essential in the development of drugs, herbicides, and other bioactive molecules. Additionally, its sulfonami

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This enables the synthesis of biaryl compounds, which are essential in the development of drugs, herbicides, and other bioactive molecules. Additionally, its sulfonamide group can contribute to the compound's role in designing molecules with specific biological activities, such as enzyme inhibition or receptor modulation. Its stability and reactivity make it a versatile tool in medicinal chemistry and material science research.

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