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(S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 2'-methoxy-6-methyl-biphenyl-2-ylmethyl ester

Base Information
  • Chemical Name:(S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 2'-methoxy-6-methyl-biphenyl-2-ylmethyl ester
  • CAS No.:94236-11-0
  • Molecular Formula:C25H23F3O4
  • Molecular Weight:444.45
  • Hs Code.:
(S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 2'-methoxy-6-methyl-biphenyl-2-ylmethyl ester

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Chemical Property of (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 2'-methoxy-6-methyl-biphenyl-2-ylmethyl ester
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Technology Process of (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 2'-methoxy-6-methyl-biphenyl-2-ylmethyl ester

There total 11 articles about (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid 2'-methoxy-6-methyl-biphenyl-2-ylmethyl ester 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:
Multi-step reaction with 9 steps
1: 1.) triethyloxonium tetrafluoroborate / 1.) 1,2-dichloroethane, 22 h; 2.) 1,2-dichloroethane, 24 h, reflux
2: 1.) Mg / 1.) ether, 1 h; 2.) ether, THF, 24 h
3: 1 M DIBAL / diethyl ether / Ambient temperature
4: tetrahydrofuran / 12 h / Ambient temperature
5: N-chlorosuccinimide / CH2Cl2 / 0.25 h
6: potassium superoxide / 18-crown-6 / diethyl ether / Ambient temperature
7: 59 percent / oxalic acid / pentane / 12 h / Ambient temperature
8: NaBH4 / ethanol / 0.5 h
9: pyridine / CCl4 / 12 h / Ambient temperature
With pyridine; potassium superoxide; sodium tetrahydroborate; N-chloro-succinimide; triethyloxonium fluoroborate; oxalic acid; diisobutylaluminium hydride; magnesium; 18-crown-6 ether; In tetrahydrofuran; tetrachloromethane; diethyl ether; ethanol; dichloromethane; pentane;
DOI:10.1021/ja00289a023
Guidance literature:
Multi-step reaction with 11 steps
1: oxalyl chloride / CH2Cl2 / 14 h
2: 30 percent NH4OH
3: 1.) triethyloxonium tetrafluoroborate / 1.) 1,2-dichloroethane, 22 h; 2.) 1,2-dichloroethane, 24 h, reflux
4: 1.) Mg / 1.) ether, 1 h; 2.) ether, THF, 24 h
5: 1 M DIBAL / diethyl ether / Ambient temperature
6: tetrahydrofuran / 12 h / Ambient temperature
7: N-chlorosuccinimide / CH2Cl2 / 0.25 h
8: potassium superoxide / 18-crown-6 / diethyl ether / Ambient temperature
9: 59 percent / oxalic acid / pentane / 12 h / Ambient temperature
10: NaBH4 / ethanol / 0.5 h
11: pyridine / CCl4 / 12 h / Ambient temperature
With pyridine; potassium superoxide; ammonium hydroxide; sodium tetrahydroborate; N-chloro-succinimide; oxalyl dichloride; triethyloxonium fluoroborate; oxalic acid; diisobutylaluminium hydride; magnesium; 18-crown-6 ether; In tetrahydrofuran; tetrachloromethane; diethyl ether; ethanol; dichloromethane; pentane;
DOI:10.1021/ja00289a023
Guidance literature:
Multi-step reaction with 10 steps
1: 30 percent NH4OH
2: 1.) triethyloxonium tetrafluoroborate / 1.) 1,2-dichloroethane, 22 h; 2.) 1,2-dichloroethane, 24 h, reflux
3: 1.) Mg / 1.) ether, 1 h; 2.) ether, THF, 24 h
4: 1 M DIBAL / diethyl ether / Ambient temperature
5: tetrahydrofuran / 12 h / Ambient temperature
6: N-chlorosuccinimide / CH2Cl2 / 0.25 h
7: potassium superoxide / 18-crown-6 / diethyl ether / Ambient temperature
8: 59 percent / oxalic acid / pentane / 12 h / Ambient temperature
9: NaBH4 / ethanol / 0.5 h
10: pyridine / CCl4 / 12 h / Ambient temperature
With pyridine; potassium superoxide; ammonium hydroxide; sodium tetrahydroborate; N-chloro-succinimide; triethyloxonium fluoroborate; oxalic acid; diisobutylaluminium hydride; magnesium; 18-crown-6 ether; In tetrahydrofuran; tetrachloromethane; diethyl ether; ethanol; dichloromethane; pentane;
DOI:10.1021/ja00289a023
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