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Aluminum, bis[2,6-bis(1,1-dimethylethyl)phenolato](2-methylpropyl)-, also known as bis(2,6-di-tert-butylphenolato)(isobutyl)aluminum, is a complex organoaluminum compound with the chemical formula C27H47AlO2. Aluminum, bis[2,6-bis(1,1-dimethylethyl)phenolato](2-methylpropyl)- is a derivative of aluminum and features two 2,6-di-tert-butylphenol ligands and an isobutyl group attached to the aluminum center. It is an organometallic compound with potential applications in various chemical reactions and processes, such as a catalyst or a reagent in the synthesis of other organoaluminum compounds. Due to its unique structure and properties, it is of interest to researchers in the field of organometallic chemistry and materials science.

136197-65-4

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136197-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136197-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,9 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136197-65:
(8*1)+(7*3)+(6*6)+(5*1)+(4*9)+(3*7)+(2*6)+(1*5)=144
144 % 10 = 4
So 136197-65-4 is a valid CAS Registry Number.

136197-65-4Relevant academic research and scientific papers

Hydrolysis of isobutylaluminum aryloxides studied by 1H NMR and quantum chemical methods

Faingol’d,Zharkov,Bravaya,Chernyak

, p. 1958 - 1965 (2017/04/03)

The results of 1H NMR and quantum chemical studies of hydrolysis of isobutylaluminum aryloxides are presented. According to the data of 1H NMR spectroscopy, the hydrolysis of monomeric diisobutylaluminum aryloxides (2,6-Bu2 t—C6H3O)AlBu2 i and (2,6-Bu2 t,4-Me—C6H2O)AlBu2 i occurs selectively at the Al—OAr bond to form the corresponding sterically bulky phenol and polyisobutylaluminoxane. At the molar ratios Al: H2O = 2, the formed sterically bulky phenol reacts slowly with diisobutylaluminum monoaryloxide to form isobutylaluminum diaryloxide. Dimeric aryloxide [(2-But—C6H4O)AlBu2 i]2 is not hydrolyzed under similar conditions. The quantum chemical calculations confirmed the experimental results: the hydrolysis at the Al—OAr bond has a lower energy barrier than that at the Al—C bond because of the formation of HH2O…OO?Ar hydrogen bonds.

Synthesis and properties of homogeneous models of the Re2O7/Al2O3 metathesis catalyst

Commereuc,Doledec

, p. 125 - 140 (2008/10/08)

Soluble complexes, including aluminum coordinated with a perrhenate and a 4-substituted-2-6-di-tert-butylphenoxy ligand or a CH2- or S-ortho bridged-4,4'-di-tert-butyldiphenoxy ligand, were synthesized and characterized. The reaction of (ArO)2Al-Cl with AgReO4 resulted in new complexes (ArO)2Al-OReO3 (A), which showed a low activity in the metathesis of 2-pentene. Complexes (ArO)2Al-R (R = isobutyl, ethyl) reacted with Re2O7 in tetrahydrofuran or dioxane, generating type B complexes including oligomeric linkages such as O3Re-[Al(OAr)-O]2-ReO3. Some of these complexes, unstable even under an argon atmosphere, were identified after stabilization with a Lewis base like quinuclidine or bipyridine. Before their stabilization, they exhibited a rather high activity in the metathesis of 2-pentene, with turnover frequency of 100/min, and functional olefins (diallylether, diallylsulfide). Upon reaction with (ArO)2Al-R in an ether solvent, A complexes might be converted into B complexes. The high activity of B complexes was associated with the presence of Al-O-Al linkages that are known to induce a powerful bidendate Lewis acidity.

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