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1-Naphthylglycolic acid

Base Information
  • Chemical Name:1-Naphthylglycolic acid
  • CAS No.:6341-54-4
  • Molecular Formula:C12H10 O3
  • Molecular Weight:202.21
  • Hs Code.:2918199090
  • NSC Number:46719
  • DSSTox Substance ID:DTXSID10286631
  • Mol file:6341-54-4.mol
1-Naphthylglycolic acid

Synonyms:1-Naphthylglycolic acid;6341-54-4;2-hydroxy-2-naphthalen-1-ylacetic acid;1-Naphthaleneglycolic acid;2-Hydroxy-2-(naphthalen-1-yl)acetic acid;NIOSH/QJ7160000;Acide alpha-naphthylphenylhydroxyacetique;alpha-Hydroxy-1-naphthaleneglycolic acid;1-Naphthaleneglycolic acid, alpha-hydroxy-;QJ71600000;Acide alpha-naphthylphenylhydroxyacetique [French];napthalene-2-oxyacetic acid;SCHEMBL1826565;SCHEMBL14376212;DTXSID10286631;AXSZGQWPAAHKDH-UHFFFAOYSA-N;NSC46719;MFCD14602012;NSC-46719;2-Hydroxy-2-(1-naphthyl)acetic Acid;AKOS010489121;SY314635;FT-0723227;EN300-1867164

Suppliers and Price of 1-Naphthylglycolic acid
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 7 raw suppliers
Chemical Property of 1-Naphthylglycolic acid
Chemical Property:
  • Vapor Pressure:4.04E-08mmHg at 25°C 
  • Melting Point:80 °C 
  • Boiling Point:428.9°C at 760 mmHg 
  • PKA:3.42±0.30(Predicted) 
  • Flash Point:227.3°C 
  • PSA:57.53000 
  • Density:1.354g/cm3 
  • LogP:1.95780 
  • XLogP3:2.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:202.062994177
  • Heavy Atom Count:15
  • Complexity:239
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2C(C(=O)O)O
Technology Process of 1-Naphthylglycolic acid

There total 7 articles about 1-Naphthylglycolic acid 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:
With methyl iodide; sodium sulfide; In water; isopropyl alcohol; at 20 ℃; for 20h;
DOI:10.1246/bcsj.61.4151
Guidance literature:
With calcium hydroxide; dicobalt octacarbonyl; methyl iodide; In ethanol; water; for 20h; Title compound not separated from byproducts; Ambient temperature;
DOI:10.1021/jo00388a060
Guidance literature:
With calcium hydroxide; dicobalt octacarbonyl; methyl iodide; In ethanol; water; for 20h; Title compound not separated from byproducts; Ambient temperature;
DOI:10.1021/jo00388a060
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