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C42H50O9

Base Information
  • Chemical Name:C42H50O9
  • CAS No.:1265446-76-1
  • Molecular Formula:C42H50O9
  • Molecular Weight:698.854
  • Hs Code.:
C<sub>42</sub>H<sub>50</sub>O<sub>9</sub>

Synonyms:

Suppliers and Price of C42H50O9
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Chemical Property of C42H50O9
Chemical Property:
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Technology Process of C42H50O9

There total 6 articles about C42H50O9 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:
C42H52O10; With ortho-nitrophenyl selenocyanate; tributylphosphine; In tetrahydrofuran; at 0 - 20 ℃;
With dihydrogen peroxide; In tetrahydrofuran; water; at 0 - 20 ℃;
DOI:10.1021/np100729d
Guidance literature:
Multi-step reaction with 5 steps
1.1: triethyl borane; tri-n-butyl-tin hydride / tetrahydrofuran; toluene / 5 h / -40 - -15 °C / in air
2.1: pyridine; trifluoroacetic anhydride / acetonitrile / 7 h / 0 °C
3.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C
3.2: 0.5 h / 0 °C
4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C
5.1: ortho-nitrophenyl selenocyanate; tributylphosphine / tetrahydrofuran / 0 - 20 °C
5.2: 0 - 20 °C
With pyridine; ortho-nitrophenyl selenocyanate; triethyl borane; tributylphosphine; potassium tert-butylate; tetrabutyl ammonium fluoride; tri-n-butyl-tin hydride; trifluoroacetic anhydride; In tetrahydrofuran; toluene; acetonitrile; 2.1: Pummerer reaction / 2.2: Pummerer reaction / 3.1: Wittig reaction / 3.2: Wittig reaction;
DOI:10.1021/np100729d
Guidance literature:
Multi-step reaction with 7 steps
1.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / -30 - 0 °C
2.1: methyllithium / tetrahydrofuran; diethyl ether / -78 - 20 °C
2.2: Inert atmosphere
3.1: triethyl borane; tri-n-butyl-tin hydride / tetrahydrofuran; toluene / 5 h / -40 - -15 °C / in air
4.1: pyridine; trifluoroacetic anhydride / acetonitrile / 7 h / 0 °C
5.1: potassium tert-butylate / tetrahydrofuran / 0.5 h / 0 °C
5.2: 0.5 h / 0 °C
6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C
7.1: ortho-nitrophenyl selenocyanate; tributylphosphine / tetrahydrofuran / 0 - 20 °C
7.2: 0 - 20 °C
With pyridine; ortho-nitrophenyl selenocyanate; triethyl borane; tributylphosphine; potassium tert-butylate; tetrabutyl ammonium fluoride; methyllithium; tri-n-butyl-tin hydride; trifluoroacetic anhydride; In tetrahydrofuran; diethyl ether; toluene; acetonitrile; 4.1: Pummerer reaction / 4.2: Pummerer reaction / 5.1: Wittig reaction / 5.2: Wittig reaction;
DOI:10.1021/np100729d
upstream raw materials:

C67H86O10SeSi2

C70H80O11SSeSi

C64H76O11SSi

C58H70O10Si

Downstream raw materials:

C40H46O9

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