Benzamide, 4,4'-(2,5-furandiyl)bis[N-methyl-

Base Information

Chemical Name:Benzamide, 4,4'-(2,5-furandiyl)bis[N-methyl-
CAS No.:199918-98-4
Molecular Formula:C20H18N2O3
Molecular Weight:334.375
Hs Code.:
DSSTox Substance ID:DTXSID00442587
Wikidata:Q82259945

Synonyms:199918-98-4;4,4'-(Furan-2,5-diyl)bis(N-methylbenzamide);Benzamide, 4,4'-(2,5-furandiyl)bis[N-methyl-;DTXSID00442587

Suppliers and Price of Benzamide, 4,4'-(2,5-furandiyl)bis[N-methyl-

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 Benzamide, 4,4'-(2,5-furandiyl)bis[N-methyl-

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:334.13174244
Heavy Atom Count:25
Complexity:424

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC(=O)C1=CC=C(C=C1)C2=CC=C(O2)C3=CC=C(C=C3)C(=O)NC

Technology Process of Benzamide, 4,4'-(2,5-furandiyl)bis[N-methyl-

There total 3 articles about Benzamide, 4,4'-(2,5-furandiyl)bis[N-methyl- 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: 80.0%

: 74-89-5
methylamine

: 101579-34-4
2,5-bis[4-carboxyphenyl]furan diacid chloride

: 199918-98-4
2,5-bis[4-(N-methylcarbamoyl)phenyl]furan

Guidance literature:: In dichloromethane; for 7h; Ambient temperature;
DOI:10.1021/jm970570i

Reference yield:

: 55368-37-1
4,4’-(furan-2,5-diyl)dibenzonitrile

: 199918-98-4
2,5-bis[4-(N-methylcarbamoyl)phenyl]furan

Guidance literature:: Multi-step reaction with 3 steps

1: 75 percent / 30percent aq. NaOH / methanol / 40 h / Heating

2: 84 percent / SOCl₂ / benzene / 2.5 h / Heating

3: 80 percent / CH₂Cl₂ / 7 h / Ambient temperature

With sodium hydroxide; thionyl chloride; In methanol; dichloromethane; benzene;
DOI:10.1021/jm970570i

Reference yield:

: 194298-15-2
2,5-bis(4-carboxyphenyl)furan

: 199918-98-4
2,5-bis[4-(N-methylcarbamoyl)phenyl]furan

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / SOCl₂ / benzene / 2.5 h / Heating

2: 80 percent / CH₂Cl₂ / 7 h / Ambient temperature

With thionyl chloride; In dichloromethane; benzene;
DOI:10.1021/jm970570i