AA20346
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 96% | in stock | $278.00 | $195.00 | - + | |
5g | 96% | in stock | $1,056.00 | $740.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA20346 |
Chemical Name: | 1,3-Dimethyluracil-5-trifluoroborate potassium salt |
CAS Number: | 1150654-77-5 |
Molecular Formula: | C6H7BF3KN2O2 |
Molecular Weight: | 246.0365 |
MDL Number: | MFCD09271782 |
SMILES: | O=c1n(C)c(=O)n(cc1[B-](F)(F)F)C.[K+] |
Complexity: | 331 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 15 |
Hydrogen Bond Acceptor Count: | 6 |
Potassium (1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)trifluoroborate is a versatile chemical compound widely used in chemical synthesis. This compound serves as a valuable source of trifluoroborate functionality in organic reactions, particularly in transition metal-catalyzed cross-coupling reactions. With its unique structure and reactivity, Potassium (1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)trifluoroborate enables the efficient construction of complex molecular structures through bond formation processes.In the field of organic chemistry, Potassium (1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)trifluoroborate is commonly employed as a key building block for the synthesis of pharmaceuticals, agrochemicals, and materials. Its use in transition metal-catalyzed reactions, such as Suzuki-Miyaura cross-coupling, allows for the selective introduction of the trifluoroborate moiety into target molecules, facilitating the creation of diverse molecular architectures efficiently.Moreover, Potassium (1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-yl)trifluoroborate exhibits excellent compatibility with a wide range of functional groups and reaction conditions, making it a valuable tool for chemists working in the field of synthetic organic chemistry. Its controlled reactivity and high functional group tolerance make it an essential component in the toolkit of synthetic chemists striving to streamline the synthesis of complex organic compounds.