Weight | 112.213 g/mol |
---|---|
Formula | C4H9KO |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Potassium tert-butoxide (865-47-4)
Score:
#2547 in Biochemistry
,
#6340 in Chemistry
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- Potassium tert-Butoxide Promoted Intramolecular Arylation via a Radical Pathway (Organic Letters, 2011)
- Phase-transfer alkylation of heterocycles in the presence of 18-crown-6 and potassium tert-butoxide (Journal of Organic Chemistry, 1980)
- MizorokiHeck-Type Reaction Mediated by Potassium tert-Butoxide (Angewandte Chemie, 2011)
- Use of potassium tert-butoxide in the methylation of carbohydrates (Carbohydrate Research, 1980)
- The super-basic butyllithium/potassium tert-butoxide mixture and other LICKOR reagents (Tetrahedron Letters, 1984)
- The Wittig Reaction Using Potassium-tert-butoxide High Yield Methylenations of Sterically Hindered Ketones (Synthetic Communications, 1985)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)[O-].[K+]
-
InChIKeyLPNYRYFBWFDTMA-UHFFFAOYSA-N
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