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Technology Process of 2-(4-Fluorophenyl)-5-(2-naphthyl)-1,3,4-oxadiazole

2-(4-Fluorophenyl)-5-(2-naphthyl)-1,3,4-oxadiazole

Base Information
  • Chemical Name:2-(4-Fluorophenyl)-5-(2-naphthyl)-1,3,4-oxadiazole
  • CAS No.:38736-15-1
  • Molecular Formula:C18H11FN2O
  • Molecular Weight:290.2911
  • Hs Code.:
  • European Community (EC) Number:254-111-6
  • NSC Number:90374
  • DSSTox Substance ID:DTXSID90192024
  • Nikkaji Number:J319.835I
  • Wikidata:Q83064618
  • ChEMBL ID:CHEMBL1706367
  • Mol file:38736-15-1.mol
2-(4-Fluorophenyl)-5-(2-naphthyl)-1,3,4-oxadiazole

Synonyms:2-(4-Fluorophenyl)-5-(2-naphthyl)-1,3,4-oxadiazole;38736-15-1;MLS002694978;EINECS 254-111-6;SMR001560891;2-(4-fluorophenyl)-5-naphthalen-2-yl-1,3,4-oxadiazole;NSC90374;cid_96845;C18H11FN2O;CHEMBL1706367;DTXSID90192024;BDBM114821;HMS3092E09;NSC 90374;NSC-90374;2-(4-fluorophenyl)-5-(2-naphthalenyl)-1,3,4-oxadiazole

Suppliers and Price of 2-(4-Fluorophenyl)-5-(2-naphthyl)-1,3,4-oxadiazole
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
  • 2-(4-FLUOROPHENYL)-5-(2-NAPHTHYL)-1,3,4-OXADIAZOLE 95.00%
  • 5MG
  • $ 503.76
Total 7 raw suppliers
Chemical Property of 2-(4-Fluorophenyl)-5-(2-naphthyl)-1,3,4-oxadiazole
Chemical Property:
  • Vapor Pressure:1.81E-08mmHg at 25°C 
  • Boiling Point:467.5°C at 760 mmHg 
  • Flash Point:236.5°C 
  • PSA：38.92000 
  • Density:1.275g/cm3 
  • LogP:4.69590 
  • XLogP3:4.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:290.08554114
  • Heavy Atom Count:22
  • Complexity:372
Purity/Quality:

99% *data from raw suppliers

2-(4-FLUOROPHENYL)-5-(2-NAPHTHYL)-1,3,4-OXADIAZOLE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C=C(C=CC2=C1)C3=NN=C(O3)C4=CC=C(C=C4)F
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