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2,6-Diethyl-3,4-dihydro-3,5-dimethyl-2H-pyran

Base Information Edit
  • Chemical Name:2,6-Diethyl-3,4-dihydro-3,5-dimethyl-2H-pyran
  • CAS No.:77372-64-6
  • Molecular Formula:C11H20O
  • Molecular Weight:168.279
  • Hs Code.:
  • Mol file:77372-64-6.mol
2,6-Diethyl-3,4-dihydro-3,5-dimethyl-2H-pyran

Synonyms:2H-Pyran,2,6-diethyl-3,4-dihydro-3,5-dimethyl-, (2S-cis)-; Anhydroserricornin;Serricornin, anhydro-

Suppliers and Price of 2,6-Diethyl-3,4-dihydro-3,5-dimethyl-2H-pyran
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2,6-Diethyl-3,4-dihydro-3,5-dimethyl-2H-pyran Edit
Chemical Property:
  • PSA:9.23000 
  • LogP:3.50540 
Purity/Quality:
Safty Information:
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MSDS Files:

SDS file from LookChem

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Technology Process of 2,6-Diethyl-3,4-dihydro-3,5-dimethyl-2H-pyran

There total 10 articles about 2,6-Diethyl-3,4-dihydro-3,5-dimethyl-2H-pyran 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 7 steps
1: 1.) yeast: Levure Alsacienne/sugar / 2.) Raney-Ni / !.) water/methanol, 3 d, 2.) methanol, reflux
2: imidazole / dimethylformamide / 36 h / 20 °C
3: 92 percent / DIBAH / diethyl ether; hexane / 12 h / -70 - 0 °C
4: N,N'-dicyclohexyl-N-methylcarbodiimidium iodide / tetrahydrofuran / 62 h / 60 °C
5: 1.) diisopropylamine/n-butyl lithium / 1.) THF/hexane, 45 min, -78 deg C, 2.) HMPA, 16 h, from -78 deg C to room temp; 1 d, room temp.
6: 1 M tetra-n-butyl ammonium fluoride / tetrahydrofuran / 16 h / Ambient temperature
7: p-toluenesulfonic acid / 80 - 160 °C / 12 Torr
With 1H-imidazole; n-butyllithium; yeast: Levure Alsacienne; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; N,N'-dicyclohexyl-N-methylcarbodiimidium iodide; toluene-4-sulfonic acid; diisopropylamine; Sucrose; nickel; In tetrahydrofuran; diethyl ether; hexane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 4 steps
1: N,N'-dicyclohexyl-N-methylcarbodiimidium iodide / tetrahydrofuran / 62 h / 60 °C
2: 1.) diisopropylamine/n-butyl lithium / 1.) THF/hexane, 45 min, -78 deg C, 2.) HMPA, 16 h, from -78 deg C to room temp; 1 d, room temp.
3: 1 M tetra-n-butyl ammonium fluoride / tetrahydrofuran / 16 h / Ambient temperature
4: p-toluenesulfonic acid / 80 - 160 °C / 12 Torr
With n-butyllithium; tetrabutyl ammonium fluoride; N,N'-dicyclohexyl-N-methylcarbodiimidium iodide; toluene-4-sulfonic acid; diisopropylamine; In tetrahydrofuran;
Guidance literature:
Multi-step reaction with 6 steps
1: imidazole / dimethylformamide / 36 h / 20 °C
2: 92 percent / DIBAH / diethyl ether; hexane / 12 h / -70 - 0 °C
3: N,N'-dicyclohexyl-N-methylcarbodiimidium iodide / tetrahydrofuran / 62 h / 60 °C
4: 1.) diisopropylamine/n-butyl lithium / 1.) THF/hexane, 45 min, -78 deg C, 2.) HMPA, 16 h, from -78 deg C to room temp; 1 d, room temp.
5: 1 M tetra-n-butyl ammonium fluoride / tetrahydrofuran / 16 h / Ambient temperature
6: p-toluenesulfonic acid / 80 - 160 °C / 12 Torr
With 1H-imidazole; n-butyllithium; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; N,N'-dicyclohexyl-N-methylcarbodiimidium iodide; toluene-4-sulfonic acid; diisopropylamine; In tetrahydrofuran; diethyl ether; hexane; N,N-dimethyl-formamide;
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