Product Name:(1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid
IUPAC Name:{1-[(tert-butoxy)carbonyl]-4-fluoro-1H-indol-2-yl}boronic acid
| Packing Unit | Available Stock | Price($) | Quantity |
|---|---|---|---|
| CM130208-1g | in stock | ƞŔǯ |
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| CM130208-5g | in stock | ňŭƞ |
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| Product Overview |
1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid (1000068-25-6) is a synthetic organic compound that has been used in a variety of scientific research applications. Its structure consists of a boronic acid group attached to an indole ring, with a tertiary butoxycarbonyl group and a fluorine atom attached to the ring. (1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid is a versatile compound that has been used in a variety of fields, including biochemistry, medicinal chemistry, and materials science. |
| Chemical Properties |
(1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid is a reactive compound, often utilized as a starting material or intermediate in various chemical reactions and synthesis processes. |
| Synthesis and Application |
1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid has been used in a variety of scientific research applications, including biochemistry, medicinal chemistry, and materials science. In biochemistry, 1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid has been used as a substrate for enzyme-catalyzed reactions, such as the synthesis of peptides and proteins. In medicinal chemistry, 1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid has been used in the synthesis of drug molecules, such as small-molecule inhibitors of protein-protein interactions. In materials science, 1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid has been used in the synthesis of polymers and other materials. |
| Storage and Handling |
Store 1-(tert-Butoxycarbonyl)-4-fluoro-1H-indol-2-yl)boronic acid under inert atmosphere in freezer under -20°C. |
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