(+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide

Base Information

Chemical Name:(+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide
CAS No.:137101-99-6
Molecular Formula:C₂₈H₃₃N₃O₂
Molecular Weight:443.589
Hs Code.:

Synonyms:(+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide

Suppliers and Price of (+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide

There total 5 articles about (+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide 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:

Reference yield: 66.0%

: 28178-42-9
2,6-diisopropylphenyl isocyanate

: 137102-00-2
(+/-)-N-(2-amino-1-phenylethyl)benzamide

: 137101-99-6
(+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide

Guidance literature:: In tetrahydrofuran; for 2h; Ambient temperature;
DOI:10.1021/jm00038a010

Reference yield:

: 5692-26-2,6485-60-5
(+/-)-N-(cyanophenylmethyl)benzamide

: 137101-99-6
(+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / NH₃, H₂ / Ranney nickel / methanol / 2585.7 Torr / Ambient temperature

2: 66 percent / tetrahydrofuran / 2 h / Ambient temperature

With ammonia; hydrogen; ranney nickel; In tetrahydrofuran; methanol;
DOI:10.1021/jm00038a010

Reference yield:

: 98-88-4
benzoyl chloride

: 137101-99-6
(+/-)-N-<2-<<<<2,6-bis(1-methylethyl)phenyl>amino>carbonyl>amino>-1-phenylethyl>benzenecarboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: 94 percent / Et₃N / tetrahydrofuran / 2 h / Ambient temperature

2: 95 percent / NH₃, H₂ / Ranney nickel / methanol / 2585.7 Torr / Ambient temperature

3: 66 percent / tetrahydrofuran / 2 h / Ambient temperature

With ammonia; hydrogen; triethylamine; ranney nickel; In tetrahydrofuran; methanol;
DOI:10.1021/jm00038a010