N-[2-chloro-5-(trifluoromethyl)phenyl]-7-methoxy-2-oxo-chromene-3-carboxamide

Base Information

Chemical Name:N-[2-chloro-5-(trifluoromethyl)phenyl]-7-methoxy-2-oxo-chromene-3-carboxamide
CAS No.:7047-16-7
Molecular Formula:C₉H₈ClNOS₂
Molecular Weight:245.754
Hs Code.:
DSSTox Substance ID:DTXSID70414115
Wikidata:Q82222735

Synonyms:7047-16-7;N-[2-chloro-5-(trifluoromethyl)phenyl]-7-methoxy-2-oxo-chromene-3-carboxamide;DTXSID70414115;AKOS002728609

Suppliers and Price of N-[2-chloro-5-(trifluoromethyl)phenyl]-7-methoxy-2-oxo-chromene-3-carboxamide

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 1 raw suppliers

Chemical Property of N-[2-chloro-5-(trifluoromethyl)phenyl]-7-methoxy-2-oxo-chromene-3-carboxamide

Chemical Property:

Vapor Pressure:8.12E-13mmHg at 25°C
Boiling Point:565.7°Cat760mmHg
Flash Point:295.9°C
Density:1.511g/cm³
XLogP3:4.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:3
Exact Mass:397.0328700
Heavy Atom Count:27
Complexity:624

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:COC1=CC2=C(C=C1)C=C(C(=O)O2)C(=O)NC3=C(C=CC(=C3)C(F)(F)F)Cl

Technology Process of N-[2-chloro-5-(trifluoromethyl)phenyl]-7-methoxy-2-oxo-chromene-3-carboxamide

There total 3 articles about N-[2-chloro-5-(trifluoromethyl)phenyl]-7-methoxy-2-oxo-chromene-3-carboxamide 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:

: 609-66-5
2-chlorobenzamide

: 7047-16-7
(2-chloro-benzoyl)-dithiocarbamic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) NaH / 1.) DMF, -10 to -20 deg C, 30 min; 2.) DMF, cooling, 30 min

With sodium hydride;