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(HC[(CMe)(N-2,6-iPr2C6H3)]2)Al(OH)2

Base Information Edit
  • Chemical Name:(HC[(CMe)(N-2,6-iPr2C6H3)]2)Al(OH)2
  • CAS No.:552812-70-1
  • Molecular Formula:C29H43AlN2O2
  • Molecular Weight:478.654
  • Hs Code.:
  • Mol file:552812-70-1.mol
(HC[(CMe)(N-2,6-iPr<sub>2</sub>C<sub>6</sub>H<sub>3</sub>)]2)Al(OH)2

Synonyms:(HC[(CMe)(N-2,6-iPr2C6H3)]2)Al(OH)2

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Chemical Property of (HC[(CMe)(N-2,6-iPr2C6H3)]2)Al(OH)2 Edit
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Technology Process of (HC[(CMe)(N-2,6-iPr2C6H3)]2)Al(OH)2

There total 5 articles about (HC[(CMe)(N-2,6-iPr2C6H3)]2)Al(OH)2 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With 1,3-di-tert-butylimidazol-2-ylidene; In water; benzene; byproducts: 1,3-di-tert-butylimidazol-2-ylidene hydrochloride; (Ar or N2); H2O added quickly to soln. of Al-complex and carbene cooled to -10 °C, suspn. stirred for 10 min.; ppt. filtered, washed twice with benzene, volatiles removed in vac., solid residue treated twice with cold pentane, filtered, dried in vac.; elem. anal.;
DOI:10.1002/anie.200353541
Guidance literature:
In hexane; toluene; addn. of soln. of water in toluene to soln. of aluminium compd. in hexane at -78°C, warming to room temp.; evapn., recrystn. (hexane) at -20°C to yield first product, elem.anal.; repeating recrystn. (hexane) to yield second product, NMR;
DOI:10.1021/om070028k
Guidance literature:
With H2O; KH; In ammonia; toluene; NH3 (liquid); ammonia condensed onto stirred suspn. of (HC((CCH3)((CH(CH3)2)2C6H3N))2)AlI2, KOH with 10-15% H2O, and KH in toluene at -78°C, stirred for 1 h, excess ammonia evapd. over 4 h, warmed slowly to room temp.; filtered, concd. under vacuo, hexane added, kept at -20°C for 1 wk, crystals sepd., further crop of crystals by evapn. of mother liquor, dissolving residue in hexane and cooling the soln. at -20°C for 2d; elem. anal.;
DOI:10.1002/anie.200390297
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