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Acetamide, 2-[[[(1R,2R,3S,5S)-3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct- 2-yl]methyl][2-[[(4-methoxyphenyl)methyl]thio]ethyl]amino]-N-[2-[[(4-meth oxyphenyl)methyl]thio]ethyl]-

Base Information
  • Chemical Name:Acetamide, 2-[[[(1R,2R,3S,5S)-3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct- 2-yl]methyl][2-[[(4-methoxyphenyl)methyl]thio]ethyl]amino]-N-[2-[[(4-meth oxyphenyl)methyl]thio]ethyl]-
  • CAS No.:189950-07-0
  • Molecular Formula:C37H48ClN3O3S2
  • Molecular Weight:682.391
  • Hs Code.:
Acetamide,
2-[[[(1R,2R,3S,5S)-3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct-
2-yl]methyl][2-[[(4-methoxyphenyl)methyl]thio]ethyl]amino]-N-[2-[[(4-meth
oxyphenyl)methyl]thio]ethyl]-

Synonyms:

Suppliers and Price of Acetamide, 2-[[[(1R,2R,3S,5S)-3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct- 2-yl]methyl][2-[[(4-methoxyphenyl)methyl]thio]ethyl]amino]-N-[2-[[(4-meth oxyphenyl)methyl]thio]ethyl]-
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Acetamide, 2-[[[(1R,2R,3S,5S)-3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct- 2-yl]methyl][2-[[(4-methoxyphenyl)methyl]thio]ethyl]amino]-N-[2-[[(4-meth oxyphenyl)methyl]thio]ethyl]-
Chemical Property:
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Technology Process of Acetamide, 2-[[[(1R,2R,3S,5S)-3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct- 2-yl]methyl][2-[[(4-methoxyphenyl)methyl]thio]ethyl]amino]-N-[2-[[(4-meth oxyphenyl)methyl]thio]ethyl]-

There total 5 articles about Acetamide, 2-[[[(1R,2R,3S,5S)-3-(4-chlorophenyl)-8-methyl-8-azabicyclo[3.2.1]oct- 2-yl]methyl][2-[[(4-methoxyphenyl)methyl]thio]ethyl]amino]-N-[2-[[(4-meth oxyphenyl)methyl]thio]ethyl]- 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 2 steps
1: Et3N / CH2Cl2 / -78 - 20 °C
2: 53 percent / Et3N / acetonitrile / 12 h / Heating
With triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/jm960532j
Guidance literature:
Multi-step reaction with 4 steps
1: (COCl)2 / CH2Cl2 / 1.5 h / Ambient temperature
2: Et3N / CH2Cl2 / 6 h / Ambient temperature
3: 79 percent / BH3*THF / 12 h / Heating
4: 53 percent / Et3N / acetonitrile / 12 h / Heating
With borane-THF; oxalyl dichloride; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/jm960532j
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