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C27H30N2O4

Base Information
  • Chemical Name:C27H30N2O4
  • CAS No.:132143-02-3
  • Molecular Formula:C27H30N2O4
  • Molecular Weight:446.546
  • Hs Code.:
C<sub>27</sub>H<sub>30</sub>N<sub>2</sub>O<sub>4</sub>

Synonyms:C27H30N2O4

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Chemical Property of C27H30N2O4
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Technology Process of C27H30N2O4

There total 13 articles about C27H30N2O4 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 11 steps
1: Et3N / DMAP / CH2Cl2 / 0 deg C to room temperature
2: 95 percent / H2 / 10percent Pd/C / toluene; ethanol / 18 h / 760 Torr
3: toluene / Ambient temperature
4: 1.5 M n-BuLi / 2-methyl-propan-2-ol; tetrahydrofuran; hexane; toluene / 0.5 h / 5 °C
5: toluene
6: 20percent aq. HCl / ethanol / Ambient temperature
7: 98 percent / dimethyl azodicarboxylate, triphenylphosphine / tetrahydrofuran / Ambient temperature
8: 54 percent / NaBH4, 2 N H2SO4 / ethanol / 0 °C
9: 1.) Et3N, MeSO2Cl / 1.) THF, -30 deg C to room temperature, 15 min, 2.) 90 min
10: 69 percent / BF3*Et2O, CaH2 / CH2Cl2 / 60 h
11: 1.) ozone, 2.) dimethyl sulfide / 1.) CH2Cl2, - 78 deg C, 2.) -78 deg C to room temperature, 2 h
With hydrogenchloride; sodium tetrahydroborate; n-butyllithium; calcium hydride; dimethylsulfide; sulfuric acid; boron trifluoride diethyl etherate; hydrogen; ozone; methanesulfonyl chloride; dimethyl azodicarboxylate; triethylamine; triphenylphosphine; dmap; palladium on activated charcoal; In tetrahydrofuran; ethanol; hexane; dichloromethane; toluene; tert-butyl alcohol;
DOI:10.1016/S0040-4020(01)90540-X
Guidance literature:
Multi-step reaction with 10 steps
1: 95 percent / H2 / 10percent Pd/C / toluene; ethanol / 18 h / 760 Torr
2: toluene / Ambient temperature
3: 1.5 M n-BuLi / 2-methyl-propan-2-ol; tetrahydrofuran; hexane; toluene / 0.5 h / 5 °C
4: toluene
5: 20percent aq. HCl / ethanol / Ambient temperature
6: 98 percent / dimethyl azodicarboxylate, triphenylphosphine / tetrahydrofuran / Ambient temperature
7: 54 percent / NaBH4, 2 N H2SO4 / ethanol / 0 °C
8: 1.) Et3N, MeSO2Cl / 1.) THF, -30 deg C to room temperature, 15 min, 2.) 90 min
9: 69 percent / BF3*Et2O, CaH2 / CH2Cl2 / 60 h
10: 1.) ozone, 2.) dimethyl sulfide / 1.) CH2Cl2, - 78 deg C, 2.) -78 deg C to room temperature, 2 h
With hydrogenchloride; sodium tetrahydroborate; n-butyllithium; calcium hydride; dimethylsulfide; sulfuric acid; boron trifluoride diethyl etherate; hydrogen; ozone; methanesulfonyl chloride; dimethyl azodicarboxylate; triethylamine; triphenylphosphine; palladium on activated charcoal; In tetrahydrofuran; ethanol; hexane; dichloromethane; toluene; tert-butyl alcohol;
DOI:10.1016/S0040-4020(01)90540-X
Guidance literature:
Multi-step reaction with 11 steps
1: 93 percent / 1.5 M DIBAL-H / toluene / Ambient temperature
2: 82 percent / pyridine/CrO3 complex / CH2Cl2
3: toluene / Ambient temperature
4: 1.5 M n-BuLi / 2-methyl-propan-2-ol; tetrahydrofuran; hexane; toluene / 0.5 h / 5 °C
5: toluene
6: 20percent aq. HCl / ethanol / Ambient temperature
7: 98 percent / dimethyl azodicarboxylate, triphenylphosphine / tetrahydrofuran / Ambient temperature
8: 54 percent / NaBH4, 2 N H2SO4 / ethanol / 0 °C
9: 1.) Et3N, MeSO2Cl / 1.) THF, -30 deg C to room temperature, 15 min, 2.) 90 min
10: 69 percent / BF3*Et2O, CaH2 / CH2Cl2 / 60 h
11: 1.) ozone, 2.) dimethyl sulfide / 1.) CH2Cl2, - 78 deg C, 2.) -78 deg C to room temperature, 2 h
With pyridine; chromium(VI) oxide; hydrogenchloride; sodium tetrahydroborate; n-butyllithium; calcium hydride; dimethylsulfide; sulfuric acid; boron trifluoride diethyl etherate; diisobutylaluminium hydride; ozone; methanesulfonyl chloride; dimethyl azodicarboxylate; triethylamine; triphenylphosphine; In tetrahydrofuran; ethanol; hexane; dichloromethane; toluene; tert-butyl alcohol;
DOI:10.1016/S0040-4020(01)90540-X
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