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Propanedioic acid, [5-(benzoyloxy)-4-methoxy-3-methyl-3-pentenyl][6-[[(1,1-dimethylethyl)di phenylsilyl]oxy]-2,4-hexadienyl]-, dimethyl ester, (Z,E,Z)-

Base Information
  • Chemical Name:Propanedioic acid, [5-(benzoyloxy)-4-methoxy-3-methyl-3-pentenyl][6-[[(1,1-dimethylethyl)di phenylsilyl]oxy]-2,4-hexadienyl]-, dimethyl ester, (Z,E,Z)-
  • CAS No.:141935-65-1
  • Molecular Formula:C41H50O8Si
  • Molecular Weight:698.929
  • Hs Code.:
Propanedioic acid,
[5-(benzoyloxy)-4-methoxy-3-methyl-3-pentenyl][6-[[(1,1-dimethylethyl)di
phenylsilyl]oxy]-2,4-hexadienyl]-, dimethyl ester, (Z,E,Z)-

Synonyms:

Suppliers and Price of Propanedioic acid, [5-(benzoyloxy)-4-methoxy-3-methyl-3-pentenyl][6-[[(1,1-dimethylethyl)di phenylsilyl]oxy]-2,4-hexadienyl]-, dimethyl ester, (Z,E,Z)-
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Propanedioic acid, [5-(benzoyloxy)-4-methoxy-3-methyl-3-pentenyl][6-[[(1,1-dimethylethyl)di phenylsilyl]oxy]-2,4-hexadienyl]-, dimethyl ester, (Z,E,Z)-
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
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Technology Process of Propanedioic acid, [5-(benzoyloxy)-4-methoxy-3-methyl-3-pentenyl][6-[[(1,1-dimethylethyl)di phenylsilyl]oxy]-2,4-hexadienyl]-, dimethyl ester, (Z,E,Z)-

There total 13 articles about Propanedioic acid, [5-(benzoyloxy)-4-methoxy-3-methyl-3-pentenyl][6-[[(1,1-dimethylethyl)di phenylsilyl]oxy]-2,4-hexadienyl]-, dimethyl ester, (Z,E,Z)- 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 8 steps
1: 30 percent / SOCl2, pyridine / 1) -20 deg C, 20 min, 2) -20 to -10 deg C, 75 min
2: 1) K2CO3 / 1) MeOH, 95 min, reflux, 2) Et2O, CH2Cl2, 0 deg C, 10 min
3: DIBAL-H / CH2Cl2 / 1.25 h / -78 °C
4: 82 percent / NEt3 / CH2Cl2 / 0.75 h / 0 °C
5: 91 percent / Bu4NF / tetrahydrofuran / 2 h / Ambient temperature
6: 85 percent / NEt3 / CH2Cl2 / 0.58 h / 0 °C
7: 1) NaH, 2) KI / 1) THF, DMF, 10 min, 2) THF, DMF, 80 deg C, 6h
8: 1) NaH / 1) THF, DMF, RT, 30 min, 2) THF, DMF, RT, 43h
With pyridine; thionyl chloride; tetrabutyl ammonium fluoride; sodium hydride; diisobutylaluminium hydride; potassium carbonate; triethylamine; potassium iodide; In tetrahydrofuran; dichloromethane;
DOI:10.1055/s-1992-34151
Guidance literature:
Multi-step reaction with 4 steps
1: imidazole / tetrahydrofuran
2: PPTS / propan-2-ol
3: LiCl, MeSO2Cl, collidine
4: 1) NaH / 1) THF, DMF, RT, 30 min, 2) THF, DMF, RT, 43h
With 1H-imidazole; 2,3,5-trimethyl-pyridine; pyridinium p-toluenesulfonate; sodium hydride; methanesulfonyl chloride; lithium chloride; In tetrahydrofuran; isopropyl alcohol;
DOI:10.1055/s-1992-34151
Guidance literature:
Multi-step reaction with 5 steps
1: DIBAL-H / CH2Cl2 / -78 °C
2: imidazole / tetrahydrofuran
3: PPTS / propan-2-ol
4: LiCl, MeSO2Cl, collidine
5: 1) NaH / 1) THF, DMF, RT, 30 min, 2) THF, DMF, RT, 43h
With 1H-imidazole; 2,3,5-trimethyl-pyridine; pyridinium p-toluenesulfonate; sodium hydride; diisobutylaluminium hydride; methanesulfonyl chloride; lithium chloride; In tetrahydrofuran; dichloromethane; isopropyl alcohol;
DOI:10.1055/s-1992-34151
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