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C31H33N3O8

Base Information
  • Chemical Name:C31H33N3O8
  • CAS No.:194042-14-3
  • Molecular Formula:C31H33N3O8
  • Molecular Weight:575.618
  • Hs Code.:
C<sub>31</sub>H<sub>33</sub>N<sub>3</sub>O<sub>8</sub>

Synonyms:C31H33N3O8

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Chemical Property of C31H33N3O8
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Technology Process of C31H33N3O8

There total 24 articles about C31H33N3O8 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:
With sodium naphthalenide; In 1,2-dimethoxyethane; at -70 ℃;
DOI:10.1016/S0040-4020(97)00652-2
Guidance literature:
Multi-step reaction with 24 steps
1: 99 percent / NaH / paraffin; tetrahydrofuran / 1.) -78 deg C -> room temperature, 4 h, 2.) room temperature, 2 h
2: 21.2 g / Zn, AcOH / tetrahydrofuran; H2O / 1 h / Ambient temperature
3: Et3N / dimethylformamide / 4 h / Ambient temperature
4: 92 percent / Et3N / CH2Cl2 / 3 h / Ambient temperature
5: 94 percent / NaH, imidazole / paraffin; tetrahydrofuran / Heating
6: 98 percent / (HF)n*Py / 0.67 h / -10 °C
7: 95 percent / Dess-Martin periodinane / CH2Cl2 / 1 h / Ambient temperature
8: 1.) LiN(TMS)2, 2.) NaBH4 / 1.) THF, -78 deg C -> -5 deg C, 3 h, 2.) H2O, 0 deg C, 20 min
9: 80 percent / Et3N, DMAP / CH2Cl2 / Ambient temperature
10: 95 percent / Dess-Martin periodinane / CH2Cl2 / 1 h / Ambient temperature
11: 94 percent / (HF)n*Py / Ambient temperature
12: 63 percent / DBU / tetrahydrofuran / Ambient temperature
13: 88 percent / NaBH4 / tetrahydrofuran; H2O / 1 h / Ambient temperature
14: 75 percent / Et3N, DMAP / CH2Cl2 / 7 h / Ambient temperature
15: 85 percent / Ph3P, Pd(PPh3, octanoic acid / tetrahydrofuran / Ambient temperature
16: 66 percent / MCPBA / CH2Cl2 / 0 °C
17: 66 percent / NaHCO3 / 5 h / -5 - 10 °C
18: 90 percent / Dess-Martin periodinane / CH2Cl2 / 0.33 h / Ambient temperature
19: 85 percent / (HF)n*Py / 1.) -10 deg C -> room temperature, 2.) room temperature, 2 h
20: 88 percent / K2CO3 / methanol / 0 - 20 °C
21: 88 percent / pyridine / 0 - 20 °C
22: 93 percent / NH3 / tetrahydrofuran / 8 h / Ambient temperature
23: 85 percent / DMAP / pyridine / 15 h / Ambient temperature
24: 61 percent / sodium naphthalenide / 1,2-dimethoxy-ethane / -70 °C
With 1H-imidazole; dmap; sodium tetrahydroborate; Octanoic acid; (HF)n*Py; Pd(PPh3; ammonia; sodium naphthalenide; sodium hydride; sodium hydrogencarbonate; potassium carbonate; Dess-Martin periodane; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; lithium hexamethyldisilazane; zinc; In tetrahydrofuran; pyridine; methanol; 1,2-dimethoxyethane; dichloromethane; water; N,N-dimethyl-formamide; paraffin;
DOI:10.1016/S0040-4020(97)00652-2
Guidance literature:
Multi-step reaction with 2 steps
1: 85 percent / DMAP / pyridine / 15 h / Ambient temperature
2: 61 percent / sodium naphthalenide / 1,2-dimethoxy-ethane / -70 °C
With dmap; sodium naphthalenide; In pyridine; 1,2-dimethoxyethane;
DOI:10.1016/S0040-4020(97)00652-2
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