Product Name:(2-Fluoro-6-isopropoxyphenyl)boronic acid

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

CAS:870777-17-6
Molecular Formula:C9H12BFO3
Purity:95%+
Catalog Number:CM137244
Molecular Weight:198

Packing Unit Available Stock Price($) Quantity
CM137244-5g in stock ƻƋƱ
CM137244-10g in stock ƱȦȌ
CM137244-25g in stock ȷȦɐ

For R&D use only.

Inquiry Form

   refresh    

Product Details

CAS NO:870777-17-6
Molecular Formula:C9H12BFO3
Melting Point:-
Smiles Code:CC(OC1=C(B(O)O)C(F)=CC=C1)C
Density:
Catalog Number:CM137244
Molecular Weight:198
Boiling Point:
MDL No:MFCD06798078
Storage:

Category Infos

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.

Product Other Information

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.