N-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethyl]-2-furancarboxamide

Base Information

Chemical Name:N-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethyl]-2-furancarboxamide
CAS No.:58827-19-3
Molecular Formula:C₁₆H₂₀N₂O₄
Molecular Weight:304.346
Hs Code.:
ChEMBL ID:CHEMBL31085
DSSTox Substance ID:DTXSID501172578

Synonyms:CHEMBL31085;SCHEMBL11195243;DTXSID501172578;N-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethyl]-2-furancarboxamide;58827-19-3

Suppliers and Price of N-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethyl]-2-furancarboxamide

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-Hydroxy-3-phenoxypropyl)amino]ethyl]-2-furancarboxamide

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:9
Exact Mass:304.14230712
Heavy Atom Count:22
Complexity:321

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)OCC(CNCCNC(=O)C2=CC=CO2)O

Technology Process of N-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethyl]-2-furancarboxamide

There total 2 articles about N-[2-[(2-Hydroxy-3-phenoxypropyl)amino]ethyl]-2-furancarboxamide 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:

: 614-99-3
Ethyl 2-furoate

: 58827-19-3
Furan-2-carboxylic acid [2-(2-hydroxy-3-phenoxy-propylamino)-ethyl]-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 18 h / 100 °C

2: propan-2-ol / 4 h / Heating

In isopropyl alcohol;
DOI:10.1021/jm00354a005