405329
Ytterbium(III) trifluoromethanesulfonate hydrate
Yb 25-28 % (approx.)
Synonym(s):
Yb(OTf)3, Trifluoromethanesulfonic acid ytterbium salt, Ytterbium(III) triflate
About This Item
composition
Degree of hydration, 1-2
Yb, 25-28% (approx.)
reaction suitability
core: ytterbium
reagent type: catalyst
SMILES string
[H]O[H].FC(F)(F)S(=O)(=O)O[Yb](OS(=O)(=O)C(F)(F)F)OS(=O)(=O)C(F)(F)F
InChI
1S/3CHF3O3S.H2O.Yb/c3*2-1(3,4)8(5,6)7;;/h3*(H,5,6,7);1H2;/q;;;;+3/p-3
InChI key
BUJKNFNMGRYZBV-UHFFFAOYSA-K
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General description
Application
- Synthesis of the dihydropyrimidine (DHPM) derivative monastrol, by Biginelli cyclocondensation.
- Cross-aldol reaction between ketone and aldehyde.
- Synthesis of β-keto enol ethers.
- Synthesis of deoxypenostatin A in a novel, stereoselective intramolecular Diels-Alder reaction.
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
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
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The Friedel–Crafts acylation is the reaction of an arene with acyl chlorides or anhydrides using a strong Lewis acid catalyst. This reaction proceeds via electrophilic aromatic substitution to form monoacylated products.
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