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3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzaldehyde

Base Information Edit
  • Chemical Name:3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzaldehyde
  • CAS No.:75646-62-7
  • Molecular Formula:C12H20O
  • Molecular Weight:180.29
  • Hs Code.:
  • Mol file:75646-62-7.mol
3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzaldehyde

Synonyms:3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzaldehyde

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Chemical Property of 3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzaldehyde Edit
Chemical Property:
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Technology Process of 3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzaldehyde

There total 12 articles about 3-t-butyl-6-methyl-2,3,4,5-tetrahydrobenzaldehyde 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: 100 percent / pyridine, oxalyl chloride / benzene / 1 h / Ambient temperature
2: 99 percent / benzene / 18 h / Heating
3: 94 percent / AlCl3, LiAlH4 / diethyl ether / 1.) 0 deg C, 1.5 h, 2.) RT, 18 h
4: dimethylsulfoxide / 18 h / 45 °C
5: 92 percent / potassium t-butoxide / tetrahydrofuran / 2 h / -10 °C
6: 30percent oxalic acid / tetrahydrofuran / 0.08 h / Heating
7: KOH / methanol / 4 h / Ambient temperature
With pyridine; potassium hydroxide; lithium aluminium tetrahydride; aluminium trichloride; oxalyl dichloride; potassium tert-butylate; oxalic acid; In tetrahydrofuran; methanol; diethyl ether; dimethyl sulfoxide; benzene;
Guidance literature:
Multi-step reaction with 9 steps
1: 99 percent / Li / liquid ammonia; diethyl ether / 0.25 h / -70 °C
2: 67 percent / NaOH / H2O; ethane-1,2-diol / 45 h / Heating
3: 100 percent / pyridine, oxalyl chloride / benzene / 1 h / Ambient temperature
4: 99 percent / benzene / 18 h / Heating
5: 94 percent / AlCl3, LiAlH4 / diethyl ether / 1.) 0 deg C, 1.5 h, 2.) RT, 18 h
6: dimethylsulfoxide / 18 h / 45 °C
7: 92 percent / potassium t-butoxide / tetrahydrofuran / 2 h / -10 °C
8: 30percent oxalic acid / tetrahydrofuran / 0.08 h / Heating
9: KOH / methanol / 4 h / Ambient temperature
With pyridine; potassium hydroxide; sodium hydroxide; lithium aluminium tetrahydride; aluminium trichloride; oxalyl dichloride; potassium tert-butylate; oxalic acid; lithium; In tetrahydrofuran; methanol; diethyl ether; ammonia; water; ethylene glycol; dimethyl sulfoxide; benzene;
Guidance literature:
Multi-step reaction with 8 steps
1: 67 percent / NaOH / H2O; ethane-1,2-diol / 45 h / Heating
2: 100 percent / pyridine, oxalyl chloride / benzene / 1 h / Ambient temperature
3: 99 percent / benzene / 18 h / Heating
4: 94 percent / AlCl3, LiAlH4 / diethyl ether / 1.) 0 deg C, 1.5 h, 2.) RT, 18 h
5: dimethylsulfoxide / 18 h / 45 °C
6: 92 percent / potassium t-butoxide / tetrahydrofuran / 2 h / -10 °C
7: 30percent oxalic acid / tetrahydrofuran / 0.08 h / Heating
8: KOH / methanol / 4 h / Ambient temperature
With pyridine; potassium hydroxide; sodium hydroxide; lithium aluminium tetrahydride; aluminium trichloride; oxalyl dichloride; potassium tert-butylate; oxalic acid; In tetrahydrofuran; methanol; diethyl ether; water; ethylene glycol; dimethyl sulfoxide; benzene;
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