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233664-53-4

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233664-53-4 Structure

233664-53-4 Structure
IdentificationBack Directory
[Name]

POTASSIUM ALLYLTRIFLUOROBORATE
[CAS]

233664-53-4
[Synonyms]

POTASSIUM ALLYLTRIFLUOROBORATE
Potassiumallyltrifluoroborate,99%
Potassium allyltrifluoroborate 95%
Potassium trifluoro(prop-2-enyl)borate
Potassium (prop-2-en-1-yl)trifluoroborate
Potassium allyltrifluoroborate Potassium trifluoro(prop-2-enyl)borate
[EINECS(EC#)]

678-439-8
[Molecular Formula]

C3H5BF3.K
[MDL Number]

MFCD03840582
[MOL File]

233664-53-4.mol
[Molecular Weight]

147.97
Chemical PropertiesBack Directory
[Melting point ]

>300 °C
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

Powder
[color ]

white
[InChI]

1S/C3H5BF3.K/c1-2-3-4(5,6)7;/h2H,1,3H2;/q-1;+1
[InChIKey]

TVPZAMJXLCDMIT-UHFFFAOYSA-N
[SMILES]

[K+].F[B-](F)(F)CC=C
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

37/38-41
[Safety Statements ]

26-36/39
[WGK Germany ]

3
[HS Code ]

2931900090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Questions and Answers (Q&A)Back Directory
[Reactions]

Versatile reagent used in Lewis acid catalyzed, the high yields synthesis of homoallylic alcohols from aldehydes.
Hazard InformationBack Directory
[Uses]

Organotrifluoroborate involved in:
  • Catalytic allylboration
  • Stereoselective nucleophilic addition
  • Pd-catalyzed heterocyclizations
  • Oxidation reactions and Oxidative Mannich reactions
  • Cross-coupling reactions

Organotrifluoroborates as versatile and stable boronic acid surrogates.
Spectrum DetailBack Directory
[Spectrum Detail]

POTASSIUM ALLYLTRIFLUOROBORATE(233664-53-4)1HNMR
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