TRIMETHYLOXONIUM TETRAFLUOROBORATE

TRIMETHYLOXONIUM TETRAFLUOROBORATE
  • CAS No.:420-37-1
Other grades of this product :
TRIMETHYLOXONIUM TETRAFLUOROBORATE Basic information
Product Name:TRIMETHYLOXONIUM TETRAFLUOROBORATE
Synonyms:TRIMETHYLOXONIUM TETRAFLUOROBORATE;trimethyl-oxoniutetrafluoroborate(1-);trimethyloxonium tetrafluoroborate(1-);Trimethyloxonium tetrafluoroborate 98+%;Trimethyloxoniumtetrafluoroborate,C24%min;Trimethyloxonium tetrafluoroborate 98%;Trimethyloxoniumtetrafluoroborate,min.95%;Oxonium, trimethyl-, tetrafluoroborate(1-)
CAS:420-37-1
MF:C3H9BF4O
MW:147.91
EINECS:206-994-4
Product Categories:halometallate salts;B (Classes of Boron Compounds);Iodonium Sulfonium & Oxonium Compounds;Oxonium Compounds;Tetrafluoroborates;Alkyl Transfer;C-X Bond Formation (Non-Halogen);Synthetic Reagents
Mol File:420-37-1.mol
TRIMETHYLOXONIUM TETRAFLUOROBORATE Chemical Properties
Melting point 200 °C
storage temp. Store at +2°C to +8°C.
solubility Soluble in nitrobenzene, nitromethane, chloroform, hot acetone, liquid sulfur dioxide. Slightly soluble in dichloromethane. Insoluble in common organic solvents.
form Crystals
color White to off-white
Sensitive Moisture Sensitive
BRN 3597303
InChIKeyJDFKFXJJAIJXPP-UHFFFAOYSA-M
CAS DataBase Reference420-37-1(CAS DataBase Reference)
EPA Substance Registry SystemOxonium, trimethyl-, tetrafluoroborate(1-) (420-37-1)
Safety Information
Hazard Codes C
Risk Statements 14-34
Safety Statements 26-36/37/39-43-45
RIDADR UN 3261 8/PG 2
WGK Germany 3
3-10-21
Hazard Note Corrosive/Freeze
TSCA Yes
HazardClass 8
PackingGroup II
HS Code 29420000
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
TRIMETHYLOXONIUM TETRAFLUOROBORATE Usage And Synthesis
Chemical Propertieswhite to off-white crystals
UsesTrimethyloxonium Tetrafluoroborate is a trialkylated oxonium used as a methylation agent in organic synthesis.
UsesTrimethyloxonium tetrafluoroborate act as a avmethylating agent and activates C-X multiple bonds. It is involved in the esterification of polyfunctional carboxylic acids. It acts as a catalyst in the polymerization of cyclic sulfides and ethers. Further, it is used in Beckmann rearrangement of oximes.
UsesReagent for the methylation of hydroxyl groups recently used in a complex, multistep synthesis directed towards spirastrellolide, a marine natural product.

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