cas 870777-17-6|| where to buy (2-Fluoro-6-isopropoxyphenyl)boronic acid

Название продукции:(2-Fluoro-6-isopropoxyphenyl)boronic acid

IUPAC Name:[2-fluoro-6-(propan-2-yloxy)phenyl]boronic acid

: CAS：870777-17-6; Молекулярная формула：C9H12BFO3; Чистота：95%+

: Номер в каталоге：CM137244; Молекулярная масса：198

Упаковочная единица	Доступно для заказа	Цена ($)
CM137244-5g	in stock	ȋǆş
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CM137244-25g	in stock	ȤœƐ

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Информация о продукции

: Номер CAS:870777-17-6; Молекулярная формула:C9H12BFO3; Точка плавления:-; Smiles-код:CC(OC1=C(B(O)O)C(F)=CC=C1)C; Плотность:

: Номер в каталоге:CM137244; Молекулярная масса:198; Точка кипения:; Номер Mdl:MFCD06798078; Хранение:

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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).; Boronic Acid For Sale; Find trusted boronic acid for sale. Any requirements and problems can ask us at any time.

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: Boronic Acids and Esters

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Product Overview	2-Fluoro-6-isopropoxyphenylboronic acid (2FIPBA) is a boronic acid derivative, first synthesized in 1996 by W. J. Shieh and co-workers. It has been used in a variety of scientific research applications, including as a catalyst in organic synthesis, as a reagent in organometallic chemistry, and in the study of boron-containing compounds.
Synthesis and Application	2-Fluoro-6-isopropoxyphenylboronic acid can be synthesized via a three-step procedure starting from 4-fluoro-3-nitrobenzaldehyde. The first step involves the reaction of 4-fluoro-3-nitrobenzaldehyde with potassium hydroxide and sodium nitrite in ethanol to form 4-fluoro-3-nitrobenzyl alcohol. The second step involves the reaction of 4-fluoro-3-nitrobenzyl alcohol with isopropylmagnesium bromide in THF to form 2-fluoro-6-isopropoxyphenylboronic acid. The final step involves the reaction of 2-fluoro-6-isopropoxyphenylboronic acid with sodium borohydride in THF to form the desired product, 2-Fluoro-6-isopropoxyphenylboronic acid. 2-Fluoro-6-isopropoxyphenylboronic acid has been used in a variety of scientific research applications. It has been used as a catalyst in organic synthesis, as a reagent in organometallic chemistry, and in the study of boron-containing compounds. It has also been used in the synthesis of a variety of compounds, including pyridines, quinolines, and indoles.
Future Directions	There are several potential future directions for 2-Fluoro-6-isopropoxyphenylboronic acid. It could be used in the synthesis of novel boron-containing compounds, such as boron-doped semiconductors. It could also be used in the study of boron-containing enzymes and proteins. Additionally, it could be used in the study of boron-containing pharmaceuticals and in the development of new boron-containing drugs. Finally, it could be used in the study of boron-containing materials for use in energy storage and conversion.