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CH3OC6H4C12N2H6C6H2(C6H13)2C12N2H6C6H4OCH3

Base Information Edit
  • Chemical Name:CH3OC6H4C12N2H6C6H2(C6H13)2C12N2H6C6H4OCH3
  • CAS No.:256504-86-6
  • Molecular Formula:C56H54N4O2
  • Molecular Weight:815.07
  • Hs Code.:
  • Mol file:256504-86-6.mol
CH<sub>3</sub>OC<sub>6</sub>H<sub>4</sub>C<sub>12</sub>N<sub>2</sub>H<sub>6</sub>C<sub>6</sub>H<sub>2</sub>(C<sub>6</sub>H<sub>13</sub>)2C<sub>12</sub>N<sub>2</sub>H<sub>6</sub>C<sub>6</sub>H<sub>4</sub>OCH<sub>3</sub>

Synonyms:CH3OC6H4C12N2H6C6H2(C6H13)2C12N2H6C6H4OCH3

Suppliers and Price of CH3OC6H4C12N2H6C6H2(C6H13)2C12N2H6C6H4OCH3
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of CH3OC6H4C12N2H6C6H2(C6H13)2C12N2H6C6H4OCH3 Edit
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Technology Process of CH3OC6H4C12N2H6C6H2(C6H13)2C12N2H6C6H4OCH3

There total 3 articles about CH3OC6H4C12N2H6C6H2(C6H13)2C12N2H6C6H4OCH3 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 tetrahydrofuran; at -5 ℃;
DOI:10.1039/a907284e
Guidance literature:
Multi-step reaction with 2 steps
1: 55 percent / Na2CO3; water / Pd(PPh3)4 / ethanol; toluene / Heating
2: 32 percent / tetrahydrofuran / -5 °C
With water; sodium carbonate; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; ethanol; toluene; 1: Substitution / 2: Arylation;
DOI:10.1039/a907284e
Guidance literature:
Multi-step reaction with 2 steps
1: 55 percent / Na2CO3; water / Pd(PPh3)4 / ethanol; toluene / Heating
2: 32 percent / tetrahydrofuran / -5 °C
With water; sodium carbonate; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; ethanol; toluene; 1: Substitution / 2: Arylation;
DOI:10.1039/a907284e
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