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[(((CH3)2CH)2C6H3NC(CH3)CHC(CH3)NC6H3(CH(CH3)2)2)Ti(CH2C(CH3)3)2]

Base Information Edit
  • Chemical Name:[(((CH3)2CH)2C6H3NC(CH3)CHC(CH3)NC6H3(CH(CH3)2)2)Ti(CH2C(CH3)3)2]
  • CAS No.:543740-55-2
  • Molecular Formula:C39H63N2Ti
  • Molecular Weight:607.823
  • Hs Code.:
  • Mol file:543740-55-2.mol
[(((CH<sub>3</sub>)2CH)2C<sub>6</sub>H<sub>3</sub>NC(CH<sub>3</sub>)CHC(CH<sub>3</sub>)NC<sub>6</sub>H<sub>3</sub>(CH(CH<sub>3</sub>)2)2)Ti(CH<sub>2</sub>C(CH<sub>3</sub>)3)2]

Synonyms:[(((CH3)2CH)2C6H3NC(CH3)CHC(CH3)NC6H3(CH(CH3)2)2)Ti(CH2C(CH3)3)2]

Suppliers and Price of [(((CH3)2CH)2C6H3NC(CH3)CHC(CH3)NC6H3(CH(CH3)2)2)Ti(CH2C(CH3)3)2]
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Chemical Property of [(((CH3)2CH)2C6H3NC(CH3)CHC(CH3)NC6H3(CH(CH3)2)2)Ti(CH2C(CH3)3)2] Edit
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Technology Process of [(((CH3)2CH)2C6H3NC(CH3)CHC(CH3)NC6H3(CH(CH3)2)2)Ti(CH2C(CH3)3)2]

There total 1 articles about [(((CH3)2CH)2C6H3NC(CH3)CHC(CH3)NC6H3(CH(CH3)2)2)Ti(CH2C(CH3)3)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:
In diethyl ether; byproducts: THF, LiCl; Ti complex was reacted with Li compd. (2 equiv.) in Et2O at -35°C;
DOI:10.1021/ja034786n
Guidance literature:
In diethyl ether; N2 atm.; to a cold soln. of complex in diethyl ether at -35°C wasadded cold soln. of ferrocenium-compound in diethyl ether, the soln. wa s allowed to stir for 3 min; filtered, dried under reduced pressure, washed with pentane, extd. with diethyl ether, filtered, concd., a few drops of ((CH3)3Si)2O were added,cooled to -35°C ; elem. anal.;
DOI:10.1021/om049400b
Guidance literature:
In toluene; N2 atm.; to a soln. of complex in toluene at -35°C was added a cold toluene soln. of iodine, the mixt. was allowed to stir 15 min; the mixt. was pumped dry, dissolved in pentane, filtered, concd., cooledto -35°C; elem. anal.;
DOI:10.1021/om049400b
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