N-(4-(2-(6-Dimethylamino)benzofuranyl)phenyl)maleimide

Base Information

Chemical Name:N-(4-(2-(6-Dimethylamino)benzofuranyl)phenyl)maleimide
CAS No.:101046-20-2
Molecular Formula:C20H16 N2 O3
Molecular Weight:332.35
Hs Code.:
DSSTox Substance ID:DTXSID80143702
Nikkaji Number:J342.475H
Wikidata:Q83007683
Mol file:101046-20-2.mol

Synonyms:N-(4-(2-(6-dimethylamino)benzofuranyl)phenyl)maleimide;N-(p-(2-(6-dimethylamino)benzofuranyl)phenyl)maleimide;N-DBPM

Suppliers and Price of N-(4-(2-(6-Dimethylamino)benzofuranyl)phenyl)maleimide

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

American Custom Chemicals Corporation
AKIYAMA'S REAGENT 95.00%
5MG
$ 496.77

Total 5 raw suppliers

Chemical Property of N-(4-(2-(6-Dimethylamino)benzofuranyl)phenyl)maleimide

Chemical Property:

Melting Point:203-204 °C(Solv: acetone (67-64-1))
Boiling Point:528.8°Cat760mmHg
PKA:4.33±0.50(Predicted)
Flash Point:273.6°C
PSA：53.76000
Density:1.327g/cm³
LogP:3.66020
XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:332.11609238
Heavy Atom Count:25
Complexity:547

Purity/Quality:

99% ^*data from raw suppliers

AKIYAMA'S REAGENT 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C1=CC2=C(C=C1)C=C(O2)C3=CC=C(C=C3)N4C(=O)C=CC4=O

Technology Process of N-(4-(2-(6-Dimethylamino)benzofuranyl)phenyl)maleimide

There total 7 articles about N-(4-(2-(6-Dimethylamino)benzofuranyl)phenyl)maleimide 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: 46.0%

: 101046-18-8
N-<4-(6-dimethylamino-2-benzofuranyl)phenyl>maleamic acid

: 101046-20-2
N-phenyl>maleimide

Guidance literature:: With sodium acetate; In acetic anhydride; Heating;
DOI:10.1246/bcsj.58.2192

Reference yield:

: 41602-56-6
4-dimethylamino-2-hydroxy-benzaldehyde

: 101046-20-2
N-phenyl>maleimide

Guidance literature:: Multi-step reaction with 5 steps

1: 56 percent / KOH / ethanol / 7 h / Heating

2: 86 percent / CH₃ONa / ethanol / 0.33 h / Heating

3: 81 percent / active carbon, FeCl₃*6H₂O, hydrazine / benzene; methanol / 7 h / Heating

4: 84 percent

5: 46 percent / AcONa / acetic anhydride / Heating

With potassium hydroxide; sodium methylate; sodium acetate; iron(III) chloride; pyrographite; hydrazine; In methanol; ethanol; acetic anhydride; benzene;
DOI:10.1246/bcsj.58.2192

Reference yield:

: 96323-59-0
6-dimethylamino-2-(4-nitrophenyl)benzofuran

: 101046-20-2
N-phenyl>maleimide

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / active carbon, FeCl₃*6H₂O, hydrazine / benzene; methanol / 7 h / Heating

2: 84 percent

3: 46 percent / AcONa / acetic anhydride / Heating

With sodium acetate; iron(III) chloride; pyrographite; hydrazine; In methanol; acetic anhydride; benzene;
DOI:10.1246/bcsj.58.2192