Benzamide, 2-(cyclopropylmethoxy)-N-(((8-methyl-8-azabicyclo(3.2.1)oct-3-yl)amino)carbonyl)-, endo-

Base Information

Chemical Name:Benzamide, 2-(cyclopropylmethoxy)-N-(((8-methyl-8-azabicyclo(3.2.1)oct-3-yl)amino)carbonyl)-, endo-
CAS No.:136013-69-9
Molecular Formula:C₂₀H₂₇N₃O₃
Molecular Weight:357.453
Hs Code.:
UNII:HDD23SY4PV
Nikkaji Number:J1.287.929F,J486.015B

Synonyms:endo-N-((8-methyl-8-azabicyclo(3.2.1)octan-3-yl)aminocarbonyl)-2-cyclopropylmethoxybenzamide;WAY 100289;WAY-100289;WAY100289

Suppliers and Price of Benzamide, 2-(cyclopropylmethoxy)-N-(((8-methyl-8-azabicyclo(3.2.1)oct-3-yl)amino)carbonyl)-, endo-

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 2 raw suppliers

Chemical Property of Benzamide, 2-(cyclopropylmethoxy)-N-(((8-methyl-8-azabicyclo(3.2.1)oct-3-yl)amino)carbonyl)-, endo-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.24g/cm³
XLogP3:3.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:357.20524173
Heavy Atom Count:26
Complexity:522

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2CCC1CC(C2)NC(=O)NC(=O)C3=CC=CC=C3OCC4CC4
Isomeric SMILES:CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)NC(=O)C3=CC=CC=C3OCC4CC4

Technology Process of Benzamide, 2-(cyclopropylmethoxy)-N-(((8-methyl-8-azabicyclo(3.2.1)oct-3-yl)amino)carbonyl)-, endo-

There total 2 articles about Benzamide, 2-(cyclopropylmethoxy)-N-(((8-methyl-8-azabicyclo(3.2.1)oct-3-yl)amino)carbonyl)-, endo- 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:

: 63874-42-0
2-((cyclopropyl)methoxy)benzamide

: 136013-69-9
endo-N-<<(8-methyl-8-azabicyclo<3.2.1>octan-3-yl)amino>carbonyl>-2-(cyclopropylmethoxy)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1,2-dichloro-ethane / 19 h / 70 °C

2: toluene; tetrahydrofuran; hexane

In tetrahydrofuran; hexane; 1,2-dichloro-ethane; toluene;
DOI:10.1021/jm00087a003