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

CAS:1000068-25-6
Molecular Formula:C13H15BFNO4
Purity:97%
Catalog Number:CM130208
Molecular Weight:279.07

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Product Details

CAS NO:1000068-25-6
Molecular Formula:C13H15BFNO4
Melting Point:-
Smiles Code:CC(C)(C)OC(=O)N1C(=CC2=C1C=CC=C2F)B(O)O
Density:
Catalog Number:CM130208
Molecular Weight:279.07
Boiling Point:
MDL No:MFCD11109421
Storage:

Category Infos

Indoles
Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.
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Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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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.