4-Hydroxy-N-(3-(4,4,5-trimethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxamide

98%

Reagent Code: #90714
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CAS Number 1704081-94-6

science Other reagents with same CAS 1704081-94-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.21 g/mol
Formula C₁₇H₂₅BN₂O₄
badge Registry Numbers
MDL Number MFCD28805763
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis for constructing carbon-carbon bonds. This enables the creation of complex pharmaceutical compounds with potential therapeutic applications. Additionally, its piperidine and carboxamide moieties contribute to its role in designing compounds with enhanced pharmacokinetic properties, such as improved bioavailability and metabolic stability. Researchers often employ this chemical in the development of potential treatments for neurological disorders, cancer, and inflammatory diseases due to its structural versatility and reactivity.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿42,370.00

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4-Hydroxy-N-(3-(4,4,5-trimethyl-1,3,2-dioxaborolan-2-yl)phenyl)piperidine-1-carboxamide
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This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis for constructing carbon-carbon bonds. This enables the creation of complex pharmaceutical compounds with potential therapeutic appli

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting specific enzymes or receptors. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic synthesis for constructing carbon-carbon bonds. This enables the creation of complex pharmaceutical compounds with potential therapeutic applications. Additionally, its piperidine and carboxamide moieties contribute to its role in designing compounds with enhanced pharmacokinetic properties, such as improved bioavailability and metabolic stability. Researchers often employ this chemical in the development of potential treatments for neurological disorders, cancer, and inflammatory diseases due to its structural versatility and reactivity.

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