iso-butanol
aluminum tri-sec-butoxide
Conditions | Yield |
---|---|
unter Abdestillieren von Isopropylformiat; |
Conditions | Yield |
---|---|
In neat (no solvent) treatment of the metal with alcohol in the presence of HgCl2 or I2 as catalysts; identified by elem. anal. for Al and by comparison of the constants withpublished data; |
Conditions | Yield |
---|---|
In water addn. of water to Al(CH3CHOC2H5)3 (air), formation of hydroxide, addn. of formic acid and water, boiling and evapn., keeping at 60°C till complete evapn., drying (2 d over drierite); TGA, DTA; | 100% |
Conditions | Yield |
---|---|
In ethanol at 0℃; | 97% |
1-(4,4-dimethyl-4,5-dihydrooxazol-2-yl)naphthalen-2-ol
aluminum tri-sec-butoxide
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Schlenk technique; | 95% |
carbon monoxide
aluminum tri-sec-butoxide
2-bromomethylnaphthyl bromide
Naphthalen-2-yl-acetic acid sec-butyl ester
Conditions | Yield |
---|---|
1,5-hexadienerhodium(I)-chloride dimer In n-heptane at 75℃; for 14h; | 91% |
3-methyl-1-butyl acetate
aluminum tri-sec-butoxide
aluminium triisopentylate
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: sec-Bu-OAc; N2 atmosphere; exchange reaction (111°C); distn. of butyl ester; | 90% |
Conditions | Yield |
---|---|
With Hg2Cl2 In butan-1-ol byproducts: H2; under N2; addn. of Mg turnings and Hg2Cl2 to stirred soln. of 2 equiv. of Al(O-sec-Bu)3 in sec-butanol, refluxed (7 d); evapn. (vac.), fractional distn. at 140-165°C/0.03 Torr, elem. anal.; | 86% |
Conditions | Yield |
---|---|
Stage #1: water; aluminum tri-sec-butoxide With ammonium hydroxide In ethanol; iso-butanol at 70℃; for 25h; Stage #2: at 400℃; for 10h; Calcination; | 82% |
aluminum tri-sec-butoxide
Conditions | Yield |
---|---|
In hexane; chloroform for 72h; | 75% |
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 59 - 70℃; for 48h; | 70% |
carbon monoxide
benzyl bromide
aluminum tri-sec-butoxide
phenyl-acetic acid sec-butyl ester
Conditions | Yield |
---|---|
1,5-hexadienerhodium(I)-chloride dimer In n-heptane at 75℃; for 14h; | 68% |
2-[(S)-4-isopropyl-4,5-dihydro-oxazol-2-yl]-6-methylphenol
aluminum tri-sec-butoxide
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 1h; Inert atmosphere; Schlenk technique; | 40% |
titanium(IV) isopropylate
hafnium tetra(n-butoxide)
aluminum tri-sec-butoxide
Conditions | Yield |
---|---|
In ethanol; water Ti and Hf alkoxides in EtOH and Ca and Gd nitrates (Ca:Gd:Hf:Al:Ti=0.1:1.5:0.1:0.3:1.85) in H2O mixed for 15 min; dried; calcined at 700°C for 1 h; ball milled for 18 h in water; pelletized at 30 MPa; sinteredin air (1500°C, 96 h); detd. by energy dispersive X-ray spectrometry and X-ray diffraction; | A n/a B 2% C n/a |
titanium(IV) isopropylate
hafnium tetra(n-butoxide)
aluminum tri-sec-butoxide
Conditions | Yield |
---|---|
In ethanol; water Ti and Hf alkoxides in EtOH and Ca and Gd nitrates (Ca:Gd:Hf:Al:Ti=0.2:1.4:0.2:0.2:1.9) in H2O mixed for 15 min; dried; calcined at 700°Cfor 1 h; ball milled for 18 h in water; pelletized at 30 MPa; sintered in air (1500°C, 96 h); detd. by energy dispersive X-ray spectrometry and X-ray diffraction; | A n/a B n/a C 2% |
4-methyl-pent-3-en-2-one
aluminum tri-sec-butoxide
A
4-methyl pent-3-en-2-ol
B
4-methyl-1,3-pentadiene
C
1,3-Dimethyl-1,3-butadien
Conditions | Yield |
---|---|
at 105 - 110℃; |
Conditions | Yield |
---|---|
With 1,4-dioxane | |
With butan-1-ol | |
With benzene |
3-nitro-benzaldehyde
aluminum tri-sec-butoxide
iso-butanol
3-Nitrobenzyl alcohol
Conditions | Yield |
---|---|
With iso-butanol |
4-nitrobenzaldehdye
aluminum tri-sec-butoxide
iso-butanol
4-nitrobenzyl chloride
aluminum tri-sec-butoxide
(E)-benzalacetone
iso-butanol
ethyl (E)-1-phenylbut-1-en-3-ol
Conditions | Yield |
---|---|
With iso-butanol |
aluminum tri-sec-butoxide
2-nitro-benzaldehyde
iso-butanol
2-Nitrobenzyl alcohol
9-fluorenone
aluminum tri-sec-butoxide
iso-butanol
9-Fluorenol
(2R,5S)-menthone
aluminum tri-sec-butoxide
iso-butanol
A
(-)-menthol
B
Neomenthol
2,3-epoxy-2-methylpropionaldehyde
aluminum tri-sec-butoxide
Conditions | Yield |
---|---|
In benzene at 20℃; for 120h; | 2.9 g |
2,3-epoxy-2-methylpropionaldehyde
aluminum tri-sec-butoxide
Conditions | Yield |
---|---|
In benzene at 20℃; for 120h; |
The Aluminium tri-sec-butoxide, with the CAS registry number 2269-22-9 and EINECS registry number 218-871-2, has the systematic name of trisec-butoxyalumane. And the molecular formula of this chemical is C12H27AlO3. It is a kind of viscous colourless or pale yellow liquid, and belongs to the following product categories: Organic-metal salt; Al (Alminum) Compounds; Classes of Metal Compounds; Typical Metal Compounds; Aluminum; Micro/Nanoelectronics; Solution Deposition Precursors. What's more, it is used as active catalyst, reducer of aldehydes and ketones, gelling agent of paint and ink, and water repellent substance of woof.
The physical properties of Aluminium tri-sec-butoxide are as following: (1)#H bond acceptors: 3; (2)#H bond donors: 0; (3)#Freely Rotating Bonds: 9; (4)Polar Surface Area: 27.69 Å2.
You should be cautious while dealing with this chemical. It is a kind of flammable chemical which is harmful in contact with skin and if swallowed. What's more, there's limited evidence of a carcinogenic effect. Therefore, you had better take the following instructions: Wear suitable protective clothing, gloves and eye/face protection, and in case of contacting with eyes, rinse immediately with plenty of water and seek medical advice; Keep away from sources of ignition - No smoking; In case of accident or if you feel unwell, seek medical advice immediately (show label where possible).
You can still convert the following datas into molecular structure:
(1)SMILES: CCC(C)O[Al](OC(C)CC)OC(C)CC
(2)InChI: InChI=1/3C4H9O.Al/c3*1-3-4(2)5;/h3*4H,3H2,1-2H3;/q3*-1;+3/rC12H27AlO3/c1-7-10(4)14-13(15-11(5)8-2)16-12(6)9-3/h10-12H,7-9H2,1-6H3
(3)InChIKey: WOZZOSDBXABUFO-DYGDCWSTAN
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