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2,3-Dihydroxybenzamide

Base Information
  • Chemical Name:2,3-Dihydroxybenzamide
  • CAS No.:13189-89-4
  • Molecular Formula:C7H7 N O3
  • Molecular Weight:153.137
  • Hs Code.:2924299090
  • UNII:Z33JA2LC96
  • Nikkaji Number:J2.799.442C
  • Wikidata:Q27095251
  • Metabolomics Workbench ID:148921
  • Mol file:13189-89-4.mol
2,3-Dihydroxybenzamide

Synonyms:2,3-Dihydroxybenzamide;13189-89-4;TRENCAM-3,2-HOPO;DB1;catecholamide;,3-Bis(oxidanyl)benzamide;2,3-Dihydroxybenzamide #;Benzamide, 2,3-dihydroxy-;3-Carbamoyl-1,2-benzenediol;SCHEMBL424097;Z33JA2LC96;Benzoic amide, 2,3-dihydroxy-;DB04476;Q27095251

Suppliers and Price of 2,3-Dihydroxybenzamide
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
  • TRC
  • 2,3-Dihydroxybenzamide
  • 25mg
  • $ 165.00
  • Biosynth Carbosynth
  • 2,3-Dihydroxybenzamide
  • 100 mg
  • $ 1200.00
Total 5 raw suppliers
Chemical Property of 2,3-Dihydroxybenzamide
Chemical Property:
  • PSA:83.55000 
  • LogP:0.89700 
  • Storage Temp.:-20°C Freezer, Under inert atmosphere 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • XLogP3:0.5
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:1
  • Exact Mass:153.042593085
  • Heavy Atom Count:11
  • Complexity:160
Purity/Quality:

99% *data from raw suppliers

2,3-Dihydroxybenzamide *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC(=C(C(=C1)O)O)C(=O)N
  • Uses 2,3-Dihydroxybenzamide is a disubstituted benzamide used in the preparation of a catechol metabolite of dilevalol. 2,3-Dihydroxybenzamide is also used in the preparation of iron chelating agents.
Technology Process of 2,3-Dihydroxybenzamide

There total 2 articles about 2,3-Dihydroxybenzamide 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:
Product distribution; 3-hydroxylation (urinary metabolism) of title compound in mice;
DOI:10.1002/jps.2600770405
Guidance literature:
upstream raw materials:

salicylamide

Downstream raw materials:

2-hydroxy-6-{2-((3-iodophenyl)amino)ethoxy}-N-methylbenzamide

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