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Dibutyltin chloride

Dibutyltin. A larger data set exists for dibutyltin, including both acute and long-term test results. The lowest concentration identified was a chronic NOEC of 0.015 mg/1 for Daphnia magna exposure to dibutyltin chloride. Long-term values were available across three trophic levels, and, therefore, an uncertainty factor of 10 was considered appropriate. [Pg.41]

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

SYNS CHLORID DI-n-BUTYLCINICITY (CZECH) D.B.T.C. DIBUTYLDICHLOROTIN DIBUTYLTIN CHLORIDE DIBUTYLTIN DICHLORIDE Dl-n-BUTYLTIN DICHLORIDE DI-n-BUTYUZINN-DICHLORID (GERMAN) DICHLORODIBUTYL-STANNANE DICHLORODIBUTYLTIN... [Pg.447]

Properties Colorless liquid.. D 1.20 (20/4C) refr index 1.4903 (25C) bp 145-147C (5 mm Hg). Soluble in the common organic solvents including alcohol, heptane, benzene, and toluene insoluble in cold water, but hydrolyzes in hot water Derivation Reaction of tetrabutyltin with dibutyltin chloride. [Pg.1263]

CCRIS 6321 Chlorid di-n-butylcinicity Di-n-butyl-zinn-dichlorid Di-n-butyltin dichloride Dibutyidichloro-stannane Dibutyidichlorotin Dibu lstannium dichloride Dibutyltin chloride Dibutyltin dichloride Diohlorodibutylstannane Dichlorodibutyltin EINECS 211-670-0 HSDB 6071 NSC 2604 Stannane, dibutyldichloro- Tin, dibutyl-, dichloride. [Pg.191]

Allylation. Carbonyl compounds are converted into homoallylic alcohols with allyl bromides-tin, diallyldibutylstannane, or allyltributylstannane-dibutyltin chloride. All three protocols require the presence of Me,SiCl (although acid chlorides may replace MCjSiCl in the last reaction). [Pg.374]

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

Dihydrocephalostatin 1 was synthesized by Fuchs by forming the pyrazine core via stitching together azido-ketone and amino-methoxyimine by using dibutyltin chloride and polyvinylpyridine in benzene. What is the mechanism for the formation of this ring ... [Pg.562]

Di-n-butyltin bis (oleate). See Dibutyltin dioleate Dibutyltin chloride. See Dibutyltin dichloride Dibutyltin diacetate... [Pg.1246]

CAS 683-18-1 EINECS/ELINCS 211-670-0 Synonyms DibutyIdichlorostannane Dibutyidichlorotin Di-n-butyidichlorotin Dibutyidichlortin Dibutylstannium dichloride Dibutyltin chloride Di-n-butyltin dichloride Din-butyl tin (IV) dichloride Dichlorodibutylstannane Dichlorodibutyltin Stannane, dibutyidichloro- Tin, dibutyl-, dichloride... [Pg.1246]

The solid-phase total synthesis of (S)-zearalenone by Nicolaou et al. (372) started with the preparation of the resins 488 and 489 from the Merrifield resin (486, Scheme 9.1). Oxidation, followed by olefination of the resulting aldehyde, gave a polystyrene vinyl resin (487), which was converted into dibutyltin chloride 488. In this process, the stannylation reagent n-Bu2SnHCl was formed in situ from -Bu2SnCl2 and n-Bu2SnH2. Reduction of 488 yielded the polymer supported tin hydride 489. [Pg.95]

One major drawback of the Stille coupling in general is the presence of tin impurities in the final product. To solve this problem, polymer-bound tin reagents can be used. Her nan et al. [88] synthesized both dimethyl- and dibutyltin chloride resins, and used them in a model reaction shown in Scheme 26. Substoichiometric rather than catalytic amounts of resin 41 were needed in order to obtain acceptable yields, and the usual Stille conditions had to be optimized to fit this specific reaction. The catalytic system consisted... [Pg.109]


See other pages where Dibutyltin chloride is mentioned: [Pg.335]    [Pg.611]    [Pg.614]    [Pg.272]    [Pg.611]    [Pg.614]    [Pg.32]    [Pg.1582]    [Pg.1688]    [Pg.1689]    [Pg.1582]    [Pg.1688]    [Pg.1689]    [Pg.1616]    [Pg.510]    [Pg.246]    [Pg.254]    [Pg.268]    [Pg.295]    [Pg.890]    [Pg.375]    [Pg.819]    [Pg.821]    [Pg.204]    [Pg.97]    [Pg.141]    [Pg.176]    [Pg.552]    [Pg.552]    [Pg.254]    [Pg.215]   
See also in sourсe #XX -- [ Pg.678 ]




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