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Benzoic acid, 4-(phenylazo)-, (E)-

Base Information
  • Chemical Name:Benzoic acid, 4-(phenylazo)-, (E)-
  • CAS No.:37790-20-8
  • Molecular Formula:C13H10N2O2
  • Molecular Weight:226.235
  • Hs Code.:2927000090
  • Mol file:37790-20-8.mol
Benzoic acid, 4-(phenylazo)-, (E)-

Synonyms:4-PHENYLDIAZENYL-BENZOIC ACID;

Suppliers and Price of Benzoic acid, 4-(phenylazo)-, (E)-
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
  • 4-PHENYLDIAZENYL-BENZOIC ACID 95.00%
  • 10G
  • $ 1334.03
  • American Custom Chemicals Corporation
  • 4-PHENYLDIAZENYL-BENZOIC ACID 95.00%
  • 5G
  • $ 909.56
Total 2 raw suppliers
Chemical Property of Benzoic acid, 4-(phenylazo)-, (E)-
Chemical Property:
  • Boiling Point:418.1°Cat760mmHg 
  • Flash Point:206.7°C 
  • PSA:62.02000 
  • Density:1.19g/cm3 
  • LogP:3.80020 
Purity/Quality:

97% *data from raw suppliers

4-PHENYLDIAZENYL-BENZOIC ACID 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Benzoic acid, 4-(phenylazo)-, (E)-

There total 4 articles about Benzoic acid, 4-(phenylazo)-, (E)- 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:
Guidance literature:
In water; dimethyl sulfoxide; for 0.0333333h; Irradiation;
DOI:10.1039/c5ra27292k
Guidance literature:
With sodium hydroxide; acetic acid; Multistep reaction; 1) r.t., overnight, 2) overnight;
DOI:10.1021/jm00125a027
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