Triethyltin acetate

Trimethyltin chloride reacts with carboxylic acids at 100° to give the corresponding chloride carboxylates Me2Sn(Cl)OCOR (187, 188), and diethyltin dihydride, triethyltin hydride, hexaethylditin, and bis(triethyltin) oxide have been shown to react with lead tetraacetate to give diethyltin diacetate or triethyltin acetate, as appropriate (189). [Pg.17]

Triethyltin acetate is the most toxic organotin compound to mammals with a LD50 rat = 4 mg/kg." For comparison, the tributyltin acetate has a LD50 of -400 mg/kg." In general, the toxicity cutoff for mammals is at the butyltin, with longer chains relatively nontoxic and shorter chains somewhat toxic. ... [Pg.58]

Compared with the alkaline conditions used in the above methods, the removal of the triethylstannylic group (triethyltin) occurs for 3(5)-triethylstannylethynylpyra-zole at room temperature in CCI4 solution in the presence of acetic acid (71ZOB 2230) (Scheme 99). [Pg.48]

Synonyms Triethyltin iodide dibutyltin chloride tributyltin chloride triphenyltin acetate bis(tributyltin) oxide triphenyltin chloride... [Pg.678]

Alternative Names/Abbreviations Triethyltin iodide, dibutyltin chloride, triphenyltin acetate, bis(tributyltin) oxide, triphenyltin chloride... [Pg.253]

Tin, tributyl-, acetate. See Tributyltin acetate Tin, triethyl-, bromide. See Triethyltin bromide Tin triphenyl acetate. See Fentin acetate Tinuvin 123. See Bis-(1-octyloxy-... [Pg.4430]

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