N-(6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)methanesulfonamide

95%

Reagent Code: #87784
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CAS Number 1132940-88-5

science Other reagents with same CAS 1132940-88-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 347.24 g/mol
Formula C₁₇H₂₂BNO₄S
badge Registry Numbers
MDL Number MFCD13191641
thermostat Physical Properties
Boiling Point 507.7±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, which is widely employed in the pharmaceutical and materials science industries. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, such as active pharmaceutical ingredients (APIs) and advanced organic materials. Additionally, it can serve as a building block in the development of fluorescent probes or sensors due to its naphthalene core, which is often utilized in optical applications. Its methanesulfonamide moiety may also contribute to biological activity, making it relevant in drug discovery research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,392.00
inventory 100mg
10-20 days ฿2,637.00

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N-(6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)methanesulfonamide
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, which is widely employed in the pharmaceutical and materials science industries. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, such as active pharmaceutical ingredients (APIs) and advanced organic materials. Additionally, it can serve as a building block in the development of fluorescent probes or sensors due to its naphthalene co

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, which is widely employed in the pharmaceutical and materials science industries. Its boronate ester group makes it a valuable intermediate for constructing complex molecules, such as active pharmaceutical ingredients (APIs) and advanced organic materials. Additionally, it can serve as a building block in the development of fluorescent probes or sensors due to its naphthalene core, which is often utilized in optical applications. Its methanesulfonamide moiety may also contribute to biological activity, making it relevant in drug discovery research.

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