(4-(2-((tert-Butoxycarbonyl)(cyclohexyl)amino) ethoxy)-3-fluorophenyl)boronic acid

98%

Reagent Code: #89227
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CAS Number 1704097-41-5

science Other reagents with same CAS 1704097-41-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 381.25 g/mol
Formula C₁₉H₂₉BFNO₅
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry. It serves as a key intermediate in the development of pharmaceutical compounds, especially those targeting enzyme inhibition or receptor modulation. The boronic acid group enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in constructing complex molecules for drug discovery. Additionally, the presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its versatility in synthesizing biologically active molecules. Its application extends to the preparation of potential therapeutics for diseases such as cancer, inflammation, and metabolic disorders.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿38,520.00
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(4-(2-((tert-Butoxycarbonyl)(cyclohexyl)amino) ethoxy)-3-fluorophenyl)boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry. It serves as a key intermediate in the development of pharmaceutical compounds, especially those targeting enzyme inhibition or receptor modulation. The boronic acid group enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in constructing complex molecules for drug discovery. Additionally, the presence of the

This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry. It serves as a key intermediate in the development of pharmaceutical compounds, especially those targeting enzyme inhibition or receptor modulation. The boronic acid group enables its use in Suzuki-Miyaura cross-coupling reactions, a widely employed method for forming carbon-carbon bonds. This makes it valuable in constructing complex molecules for drug discovery. Additionally, the presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enhancing its versatility in synthesizing biologically active molecules. Its application extends to the preparation of potential therapeutics for diseases such as cancer, inflammation, and metabolic disorders.

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