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![[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)](/deepweb/assets/sigmaaldrich/product/structures/130/734/8846aa26-1858-458a-998d-8c306c13bf0f/640/8846aa26-1858-458a-998d-8c306c13bf0f.png)
form
solid
mp
45-50 °C
SMILES string
[K+].F[B-](F)(F)c1ccncc1
InChI
1S/C5H4BF3N.K/c7-6(8,9)5-1-3-10-4-2-5;/h1-4H;/q-1;+1
InChI key
SLPOSOZRTRIRQS-UHFFFAOYSA-N
Application
- Cross-coupling with unactivated alkyl halides
- C-O activation of phenol derivatives
- Suzuki-Miyaura cross-coupling reactions
Organotrifluoroborates as versatile and stable boronic acid surrogates.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
140.9 °F
Flash Point(C)
60.5 °C
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Articles
Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.
Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.
Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.
Bench-stable Potassium Organotrifluoroborates enable diverse C-C bond formation reactions.
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