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2,3-Dihydroxynaphthalene

Base Information
  • Chemical Name:2,3-Dihydroxynaphthalene
  • CAS No.:92-44-4
  • Molecular Formula:C10H8O2
  • Molecular Weight:160.172
  • Hs Code.:29072900
  • European Community (EC) Number:202-156-7
  • NSC Number:8707
  • UNII:O9U131030Z
  • DSSTox Substance ID:DTXSID2043903
  • Nikkaji Number:J30.353D
  • Wikidata:Q27117387
  • Metabolomics Workbench ID:55782
  • ChEMBL ID:CHEMBL205007
  • Mol file:92-44-4.mol
2,3-Dihydroxynaphthalene

Synonyms:2,3-dihydroxynaphthalene

Suppliers and Price of 2,3-Dihydroxynaphthalene
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-Dihydroxynaphthalene
  • 5g
  • $ 45.00
  • TCI Chemical
  • 2,3-Dihydroxynaphthalene >98.0%(GC)(T)
  • 25g
  • $ 37.00
  • TCI Chemical
  • 2,3-Dihydroxynaphthalene >98.0%(GC)(T)
  • 250g
  • $ 243.00
  • Sigma-Aldrich
  • 2,3-Dihydroxynaphthalene ≥98.0% (HPLC)
  • 250 g
  • $ 416.00
  • Sigma-Aldrich
  • 2,3-Dihydroxynaphthalene ≥98.0% (HPLC)
  • 250g-f
  • $ 246.00
  • Sigma-Aldrich
  • 2,3-Dihydroxynaphthalene ≥98.0% (HPLC)
  • 50 g
  • $ 116.00
  • Sigma-Aldrich
  • 2,3-Dihydroxynaphthalene ≥98.0% (HPLC)
  • 50g-f
  • $ 116.00
  • Sigma-Aldrich
  • 2,3-Naphthalenediol for synthesis. CAS 92-44-4, pH 6 (1 g/l, H O, 20 °C)., for synthesis
  • 8145780050
  • $ 71.80
  • Sigma-Aldrich
  • 2,3-Naphthalenediol for synthesis
  • 50 g
  • $ 68.73
  • Oakwood
  • Naphthalene-2,3-diol
  • 5g
  • $ 10.00
Total 124 raw suppliers
Chemical Property of 2,3-Dihydroxynaphthalene
Chemical Property:
  • Appearance/Colour:Off white to redish white powder 
  • Vapor Pressure:1.71E-05mmHg at 25°C 
  • Melting Point:161-165 °C(lit.) 
  • Refractive Index:1.725 
  • Boiling Point:353.9 °C at 760 mmHg 
  • PKA:9.10±0.40(Predicted) 
  • Flash Point:181 °C 
  • PSA:40.46000 
  • Density:1.33 g/cm3 
  • LogP:2.25100 
  • Storage Temp.:2-8°C 
  • Solubility.:4g/l 
  • Water Solubility.:slightly soluble 
  • XLogP3:2.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:160.052429494
  • Heavy Atom Count:12
  • Complexity:140
Purity/Quality:

99% *data from raw suppliers

2,3-Dihydroxynaphthalene *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Other Classes -> Naphthols
  • Canonical SMILES:C1=CC=C2C=C(C(=CC2=C1)O)O
  • General Description 2,3-Dihydroxynaphthalene (also known as 2,3-naphthalenediol) is a dihydroxy-substituted naphthalene derivative that has been studied for its ability to form reactive cocrystals capable of intermolecular acyl-transfer reactions in the solid state. Its molecular structure, featuring two hydroxyl groups in close proximity, facilitates favorable geometry for nucleophilic attack on electrophilic carbonyl groups in ester derivatives, enabling solid-state reactivity. 2,3-Dihydroxynaphthalene has been utilized in cocrystals with diesters, where non-covalent interactions (e.g., C-H···π) and proper alignment of reactive groups support domino-type acyl migrations, demonstrating its potential in designing functional supramolecular assemblies for solid-state reactions. Additionally, its derivatives have been employed as sensitizers in luminescent assays for enzymatic activity detection.
Technology Process of 2,3-Dihydroxynaphthalene

There total 37 articles about 2,3-Dihydroxynaphthalene 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: 95.0%

Guidance literature:
With toluene-4-sulfonic acid; In neat (no solvent, solid phase); at 20 ℃; for 0.583333h; Green chemistry;
DOI:10.2174/1570178614666170321103650
Guidance literature:
With aluminum (III) chloride; In benzene; for 5h; Reflux;
DOI:10.1055/s-0032-1318332
Guidance literature:
With 2,4,6-trimethylphenylcarbene copper; dihydrogen peroxide; trimethyldodecylammonium chloride; In octane; at 50 ℃; for 7h; Reagent/catalyst;
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