Benzamide, N,N'-1,4-phenylenebis(4-amino-

Base Information

Chemical Name:Benzamide, N,N'-1,4-phenylenebis(4-amino-
CAS No.:2362-26-7
Molecular Formula:C20H18 N4 O2
Molecular Weight:346.3825
Hs Code.:
DSSTox Substance ID:DTXSID40178292
Nikkaji Number:J814.847C
Wikidata:Q83048679
Mol file:2362-26-7.mol

Synonyms:2362-26-7;N,N'-(1,4-Phenylene)bis(4-aminobenzamide);Benzamide, N,N'-1,4-phenylenebis(4-amino-;BRN 2775086;4-amino-N-[4-[(4-aminobenzoyl)amino]phenyl]benzamide;N,N'-1,4-Phenylenebis(4-aminobenzamide);4-amino-N-{4-[(4-aminobenzoyl)amino]phenyl}benzamide;Cambridge id 5211889;Oprea1_189605;Oprea1_701234;CBDivE_007541;SCHEMBL2128727;DTXSID40178292;MFCD00368865;AKOS000670199;N,N'-p-phenylenebis(p-aminobenzamide);LS-27339;CS-0336293;EU-0066832;AB00075321-01;N,N-(1,4-PHENYLENE)BIS(4-AMINOBENZAMIDE);SR-01000389445;SR-01000389445-1

Suppliers and Price of Benzamide, N,N'-1,4-phenylenebis(4-amino-

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 6 raw suppliers

Chemical Property of Benzamide, N,N'-1,4-phenylenebis(4-amino-

Chemical Property:

Boiling Point:481.3°Cat760mmHg
Flash Point:244.9°C
Density:1.375g/cm³
XLogP3:2.2
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:346.14297583
Heavy Atom Count:26
Complexity:430

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1C(=O)NC2=CC=C(C=C2)NC(=O)C3=CC=C(C=C3)N)N

Technology Process of Benzamide, N,N'-1,4-phenylenebis(4-amino-

There total 4 articles about Benzamide, N,N'-1,4-phenylenebis(4-amino- 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:

: 5922-25-8
N,N¹-(1,4-phenylene)bis(4-nitrobenzamide)

: 2362-26-7
N,N'-(p-phenylene)bis(p-aminobenzamide)

Guidance literature:: With hydrogen; palladium on activated charcoal; In N,N-dimethyl-formamide; under 760 Torr; Ambient temperature;

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 2362-26-7
N,N'-(p-phenylene)bis(p-aminobenzamide)

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / 4percent aq. NaHCO₃ / acetone / 10 h / Ambient temperature

2: H₂ / 10percent Pd/C / dimethylformamide / 760 Torr / Ambient temperature

With hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In N,N-dimethyl-formamide; acetone;

Reference yield:

: 62-23-7
4-nitro-benzoic acid

: 2362-26-7
N,N'-(p-phenylene)bis(p-aminobenzamide)

Guidance literature:: Multi-step reaction with 3 steps

1: 93 percent / thionyl chloride / 10 h / Heating

2: 74 percent / 4percent aq. NaHCO₃ / acetone / 10 h / Ambient temperature

3: H₂ / 10percent Pd/C / dimethylformamide / 760 Torr / Ambient temperature

With thionyl chloride; hydrogen; sodium hydrogencarbonate; palladium on activated charcoal; In N,N-dimethyl-formamide; acetone;