2-Benzofurancarboxamide, 5-(piperidinomethyl)-

Base Information

Chemical Name:2-Benzofurancarboxamide, 5-(piperidinomethyl)-
CAS No.:6115-97-5
Molecular Formula:C15H18N2O2
Molecular Weight:258.3156
Hs Code.:2934999090
NSC Number:85432
DSSTox Substance ID:DTXSID80210044
Nikkaji Number:J54.518J
Wikidata:Q83084591
Mol file:6115-97-5.mol

Synonyms:5-(N-Piperidinomethyl)coumarylamide;6115-97-5;2-BENZOFURANCARBOXAMIDE, 5-(PIPERIDINOMETHYL)-;L 4035;NSC 85432;2-Benzofurancarboxamide, 5-(1-piperidinylmethyl)-;BRN 1623317;5-20-03-00423 (Beilstein Handbook Reference);NCIOpen2_005002;DTXSID80210044;NSC85432;NSC-85432;WLN: T56 BOJ CVZ G1- AT6NTJ;LS-34931;L-4035

Suppliers and Price of 2-Benzofurancarboxamide, 5-(piperidinomethyl)-

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 5 raw suppliers

Chemical Property of 2-Benzofurancarboxamide, 5-(piperidinomethyl)-

Chemical Property:

Vapor Pressure:4.49E-08mmHg at 25°C
Boiling Point:443.8°Cat760mmHg
Flash Point:222.2°C
PSA：59.47000
Density:1.221g/cm³
LogP:3.15580
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:258.136827821
Heavy Atom Count:19
Complexity:328

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCN(CC1)CC2=CC3=C(C=C2)OC(=C3)C(=O)N

Technology Process of 2-Benzofurancarboxamide, 5-(piperidinomethyl)-

There total 1 articles about 2-Benzofurancarboxamide, 5-(piperidinomethyl)- 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: