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Hydroxy(naphthalen-1-yl)phenylacetic acid

Base Information
  • Chemical Name:Hydroxy(naphthalen-1-yl)phenylacetic acid
  • CAS No.:6309-40-6
  • Molecular Formula:C18H14O3
  • Molecular Weight:278.307
  • Hs Code.:2918199090
  • NSC Number:42556
  • DSSTox Substance ID:DTXSID90285647
  • Mol file:6309-40-6.mol
Hydroxy(naphthalen-1-yl)phenylacetic acid

Synonyms:6309-40-6;hydroxy(naphthalen-1-yl)phenylacetic acid;2-HYDROXY-2-NAPHTHALEN-1-YL-2-PHENYL-ACETIC ACID;NSC42556;SCHEMBL4592642;DTXSID90285647;NSC-42556;2-Hydroxy-2-(naphthalen-1-yl)-2-phenylacetic acid

Suppliers and Price of Hydroxy(naphthalen-1-yl)phenylacetic 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 11 raw suppliers
Chemical Property of Hydroxy(naphthalen-1-yl)phenylacetic acid
Chemical Property:
  • Vapor Pressure:7.96E-11mmHg at 25°C 
  • Refractive Index:1.684 
  • Boiling Point:500.2 °C at 760 mmHg 
  • Flash Point:270.4 °C 
  • PSA:57.53000 
  • Density:1.309 g/cm3 
  • LogP:3.16030 
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:278.094294304
  • Heavy Atom Count:21
  • Complexity:375
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C(C2=CC=CC3=CC=CC=C32)(C(=O)O)O
Technology Process of Hydroxy(naphthalen-1-yl)phenylacetic acid

There total 9 articles about Hydroxy(naphthalen-1-yl)phenylacetic 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:
Multi-step reaction with 3 steps
1: aluminium chloride; 1.1.2.2-tetrachloro-ethane
2: aq.-ethanolic sodium carbonate-solution
3: diethyl ether
With aluminium trichloride; diethyl ether; sodium carbonate; 1,1,2,2-tetrachloroethane;
DOI:10.1021/ja01235a008
Guidance literature:
Multi-step reaction with 2 steps
1: aq.-ethanolic sodium carbonate-solution
2: diethyl ether
With diethyl ether; sodium carbonate;
DOI:10.1021/ja01235a008
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