N-{4-[(E)-phenyldiazenyl]phenyl}benzamide

Base Information

Chemical Name:N-{4-[(E)-phenyldiazenyl]phenyl}benzamide
CAS No.:32299-80-2
Molecular Formula:C19H15N3O
Molecular Weight:301.3419
Hs Code.:2927000090
Mol file:32299-80-2.mol

Synonyms:benzoic acid-(4-phenylazo-anilide);4-Benzoylaminoazobenzol;4'-(Phenylazo)benzanilide;N-{4-[(E)-phenyldiazenyl]phenyl}benzamide;4-Benzamino-azobenzol;Benzoesaeure-(4-phenylazo-anilid);4-Benzolazo-N-benzoyl-anilin;

Suppliers and Price of N-{4-[(E)-phenyldiazenyl]phenyl}benzamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-{4-[(E)-phenyldiazenyl]phenyl}benzamide

Chemical Property:

Vapor Pressure:7.4E-07mmHg at 25°C
Boiling Point:407.7°Cat760mmHg
Flash Point:200.4°C
PSA：53.82000
Density:1.14g/cm³
LogP:5.42730

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-{4-[(E)-phenyldiazenyl]phenyl}benzamide

There total 3 articles about N-{4-[(E)-phenyldiazenyl]phenyl}benzamide 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: 84.0%

: 98-88-4
benzoyl chloride

: 60-09-3
aniline yellow

: 32299-80-2
N-[4-(phenyldiazenyl)phenyl]benzamide

Guidance literature:: With triethylamine; at 20 ℃; for 0.166667h;
DOI:10.14233/ajchem.2015.17639

Reference yield:

: 62-53-3
aniline

: 32299-80-2
N-[4-(phenyldiazenyl)phenyl]benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: sodium nitrite; hydrogenchloride / water / 0 - 5 °C

2: triethylamine / 0.17 h / 20 °C

With hydrogenchloride; triethylamine; sodium nitrite; In water;
DOI:10.14233/ajchem.2015.17639