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420-37-1 - Trimethyloxonium tetrafluoroborate, 96% - A15175 - Alfa Aesar

A15175 Trimethyloxonium tetrafluoroborate, 96%

Numéro CAS
420-37-1
Synonymes

Dimensions Prix ($) Quantité Disponibilité
10g 56,80
50g 226,80
250g 1106,22
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Trimethyloxonium tetrafluoroborate, 96%

MDL
MFCD00011798
EINECS
206-994-4

Propriétés chimiques

Formule
C3H9BF4O
Poids formulaire
147.91
Point de fusion
ca 190° dec.
Sensibilité
Moisture Sensitive
Solubilité
Soluble in nitrobenzene, nitromethane, chloroform, hot acetone, liquid sulfur dioxide. Slightly soluble in dichloromethane. Insoluble in common organic solvents.

Applications

Trimethyloxonium 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.

Notes

Hygroscopic. Moisture sensitive. Store in a cool place. Incompatible with strong oxidizing agents and bases.

Références bibliographiques

Trialkyloxonium salts, also known as Meerwein's salts, are powerful alkylating agents under mild conditions. For general reactions of trialkyloxonium salts, see Triethyl­oxonium tetrafluoroborate, A14420 . For a brief feature of their uses in synthesis, see: Synlett, 195 (2004).

Alkylation of ethylene thioacetals proceeds only to the monoalkyl salt unless water is added, when the thioacetal is cleaved to give the carbonyl compound and the tetraalkyl ethane bis-sulfonium salt: Synthesis, 135 (1981). Alkylation on S to promote leaving group ability has also been used in a synthesis of oxiranes from ß-hydroxy sulfides: J. Am. Chem. Soc., 95, 3429 (1973); J. Chem. Soc., Chem. Commun., 714 (1975).

N,N-Dialkyl arylcarboxamides, useful as substrates for directed metallation reactions, can be converted to methyl esters in high yield: Tetrahedron, 56, 9875 (2000).

Nortcliffe, A.; Moody, C. J. Seven-membered ring scaffolds for drug discovery: Access to functionalised azepanes and oxepanes through diazocarbonyl chemistry. Bioorg. Med. Chem. 2015, 23 (11), 2730-2735.

Lim, J. Y.; Cunningham, M. J.; Davis, J. J.; Beer, P. D. Halogen bonding-enhanced electrochemical halide anion sensing by redox-active ferrocene receptors. Chem. Commun. 2015, 51 (78), 14640-14643.

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H314-H318

Causes severe skin burns and eye damage. Causes serious eye damage.

Mentions de prudence: P260-P280-P303+P361+P353-P305+P351+P338-P301+P330+P331-P304+P340-P310-P363-P405-P501a

Do not breathe dust/fume/gas/mist/vapours/spray. Wear protective gloves/protective clothing/eye protection/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Immediately call a POISON CENTER or doctor/physician. Wash contaminated clothing before reuse. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Beilstein
3597303
Classe de danger
8
Groupe d'emballage
II
Code tarifaire harmonisé
2920.90
TSCA
Yes

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