Antioxidant BHT 264
CAS:128-37-0
Purity:99%
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Product Details
Reactions |
Catalyst for the synthesis of acyclic epoxy alcohols and allylic epoxy alcohols. Useful for diastereoselective reduction of alpha-fluoroketones. Catalyzes the asymmetric allylation of ketones. Reagent for the synthesis of cyclopropylamines from aryl and alkenyl nitriles. Useful for racemic and/or enantioselective addition of nucleophiles to aldehydes, ketones and imines. Catalytic intramolecular formal [3+2] cycloaddition. Catalyst for the synthesis of cyclopropanols from esters and organomagnesium reagents |
Definition |
ChEBI: Titanium(IV) isopropoxide is a titanium coordination entity consisting of a titanium(IV) cation with four propan-2-olate anions as counterions. |
General Description |
Tetraisopropyl titanate appears as a water-white to pale-yellow liquid with an odor like isopropyl alcohol. About the same density as water. Vapors heavier than air. |
Air & Water Reactions |
Highly flammable. Fumes in air. Soluble in water. Decomposes rapidly in water to form flammable isopropyl alcohol. |
Reactivity Profile |
Metal alkyls, such as TETRAISOPROPYL TITANATE, are reducing agents and react rapidly and dangerously with oxygen and with other oxidizing agents, even weak ones. Thus, they are likely to ignite on contact with alcohols. |
Health Hazard |
Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution. |
Flammability and Explosibility |
Flammable |
Purification Methods |
Dissolve it in dry *C6H6 , filter if a solid separates, evaporate and fractionate. It is hydrolysed by H2O to give solid Ti2O(iso-OPr)2 m ca 48o. [Bradley et al. J Chem Soc 2027, 1952, Bradley et al. J Chem Soc 469 1957, Beilstein 1 II 328, 1 IV 1469S.] |
InChI:InChI=1/4C3H8O.Ti/c4*1-3(2)4;/h4*3-4H,1-2H3;
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titanium tetrachloride
isopropyl alcohol
titanium(IV) isopropylate
Conditions | Yield |
---|---|
With
diethylamine;
In
hexane;
at 0 ℃;
for 1h;
Reagent/catalyst;
Inert atmosphere;
|
85% |
With
NH3;
In
benzene;
byproducts: NH4Cl; NH4Cl sepd., Ti(OiPr)4 distilled; elem. anal.;
|
70% |
With
sodium;
byproducts: NaCl; isopropanol was placed in flask, Na was added with heating, Ti-salt was introduced; extd. with hexane, centrifuged, solvents were distilled off, vac. distillation;
|
59.7% |
With
ammonia;
In
benzene;
under N2; TiCl4 added slowly dropwise with stirring to alc. at 0°C; the resultant mixt. dild. with benzene; dry ammonia passed for 1 h; mixt. heated for 2-3 h on a water bath at 60-65°C; ppt. filtered off; distd. under vac.;
|
|
With
trimethylamine;
In
not given;
TiCl4 reacted with 2-propanol in the presence of trimethylamine;
|
2-anilinoacetophenone
titanium(IV) isopropylate
Conditions | Yield |
---|---|
With
ethylenediamine;
In
methanol;
|
sodium isopropylate
isopropyl alcohol
titanium tetrachloride
N-phenylbenzohydroxamic acid
isopropyl hydrogen maleate
(4-Diethoxymethyl-3-isopropoxy-hexyl)-benzene
(4-Chloro-5,5-diethoxy-3-isopropoxy-pentyl)-benzene
monoisopropyl phthalate