AA01996
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $17.00 | $12.00 | - + | |
1g | 97% | in stock | $31.00 | $22.00 | - + | |
5g | 97% | in stock | $154.00 | $108.00 | - + | |
10g | 97% | in stock | $307.00 | $215.00 | - + | |
25g | 97% | in stock | $704.00 | $493.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA01996 |
Chemical Name: | 3-Amino-4-fluorophenylboronic acid, pinacol ester |
CAS Number: | 1003575-43-6 |
Molecular Formula: | C12H17BFNO2 |
Molecular Weight: | 237.0783 |
MDL Number: | MFCD11044430 |
SMILES: | Fc1ccc(cc1N)B1OC(C(O1)(C)C)(C)C |
Complexity: | 282 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 4 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 1 |
2-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is a versatile compound widely used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the synthesis of various organic molecules. Specifically, it is commonly employed in Suzuki-Miyaura cross-coupling reactions to introduce the 2-fluoroaniline moiety into complex molecular structures. The presence of the boronate ester group facilitates efficient coupling with aryl halides or pseudohalides, enabling the formation of C-C bonds with high regioselectivity and functional group tolerance. Additionally, the 2-fluoro substituent enhances the reactivity and selectivity of the coupling reaction, making this compound a valuable tool for the construction of biologically active molecules, pharmaceutical intermediates, and advanced materials.