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N-acetyl-4-(o-bromophenyl)butylamine

Base Information Edit
  • Chemical Name:N-acetyl-4-(o-bromophenyl)butylamine
  • CAS No.:178809-23-9
  • Molecular Formula:C12H16BrNO
  • Molecular Weight:270.169
  • Hs Code.:
  • Mol file:178809-23-9.mol
N-acetyl-4-(o-bromophenyl)butylamine

Synonyms:N-acetyl-4-(o-bromophenyl)butylamine

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-acetyl-4-(o-bromophenyl)butylamine Edit
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Technology Process of N-acetyl-4-(o-bromophenyl)butylamine

There total 6 articles about N-acetyl-4-(o-bromophenyl)butylamine 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 triethylamine; In dichloromethane; for 2h;
DOI:10.1016/0040-4020(96)00266-9
Guidance literature:
Multi-step reaction with 6 steps
1: 81 percent / sodium bicarbonate, tetra-n-butyl ammonium chloride, palladium acetate / dimethylformamide / 18.5 h / 40 °C
2: 78 percent / NaBH4 / methanol / a) RT, 14 h, b) reflux, 3.5 h
3: 91 percent / pyridine / 0 °C
4: 62 percent / tetrahydrofuran; dimethylsulfoxide / 6 h / 65 °C
5: 75 percent / LiAlH4, AlCl3 / diethyl ether / 11 h
6: 81 percent / Et3N / CH2Cl2 / 2 h
With pyridine; sodium tetrahydroborate; lithium aluminium tetrahydride; aluminium trichloride; tetrabutyl-ammonium chloride; palladium diacetate; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/0040-4020(96)00266-9
Guidance literature:
Multi-step reaction with 4 steps
1: 91 percent / pyridine / 0 °C
2: 62 percent / tetrahydrofuran; dimethylsulfoxide / 6 h / 65 °C
3: 75 percent / LiAlH4, AlCl3 / diethyl ether / 11 h
4: 81 percent / Et3N / CH2Cl2 / 2 h
With pyridine; lithium aluminium tetrahydride; aluminium trichloride; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/0040-4020(96)00266-9
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