POTASSIUM ETHYLTRIFLUOROBORATE
Product Information
Molecular Formula
C2H5BF3K
Molecular Weight
135.97
Description
Potassium ethyltrifluoroborate can be used as a substrate in Suzuki-Miyaura coupling reaction with alkenyl bromides to produce alkene derivatives.
Synonyms
POTASSIUM ETHYLTRIFLUOROBORATE
IUPAC Name
potassiumethyl(trifluoro)boranuide
SMILES
[B-](CC)(F)(F)F.[K+]
InChI
InChI=1S/C2H5BF3.K/c1-2-3(4,5)6/h2H2,1H3/q-1+1
InChI Key
GIIPADVFWNGSKY-UHFFFAOYSA-N
Melting Point
80-84 °C
Flash Point
Not applicable
Purity
95%
Safety Information
Hazards
H315 - H319 - H335
Precautionary Statement
P302 + P352 - P305 + P351 + P338
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
0
Exact Mass
136.0073463 g/mol
Monoisotopic Mass
136.0073463 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
7
Formal Charge
0
Complexity
42.7
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-112500313-A | Method for replacing fluorination reaction of halogenated aromatic hydrocarbon | 2020-12-04 |
| WO-2022013564-A1 | Photoredox protein modification | 2020-07-16 |
| US-2020399258-A1 | Benzisoxazole Sulfonamide Derivatives | 2019-06-18 |
| WO-2020254946-A1 | Benzisoxazole sulfonamide derivatives | 2019-06-18 |
| TW-202115048-A | Benzisoxazole sulfonamide derivatives | 2019-06-18 |
| AU-2020296361-A1 | Benzisoxazole sulfonamide derivatives | 2019-06-18 |
| CA-3143666-A1 | Benzisoxazole sulfonamide derivatives | 2019-06-18 |
| US-2020190093-A1 | Substituted xanthine derivatives | 2018-12-12 |
| WO-2020120450-A1 | Substituted xanthine derivatives | 2018-12-12 |
| TW-202039495-A | Novel substituted xanthine derivatives | 2018-12-12 |
