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Benzyl naphthalen-2-yl carbonate

Base Information
  • Chemical Name:Benzyl naphthalen-2-yl carbonate
  • CAS No.:7107-60-0
  • Molecular Formula:C18H14O3
  • Molecular Weight:278.307
  • Hs Code.:
  • NSC Number:171048
  • DSSTox Substance ID:DTXSID70305534
  • Wikidata:Q82052187
Benzyl naphthalen-2-yl carbonate

Synonyms:7107-60-0;benzyl naphthalen-2-yl carbonate;NSC171048;DTXSID70305534;NSC-171048

Suppliers and Price of Benzyl naphthalen-2-yl carbonate
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
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Total 5 raw suppliers
Chemical Property of Benzyl naphthalen-2-yl carbonate
Chemical Property:
  • Vapor Pressure:3.36E-08mmHg at 25°C 
  • Boiling Point:447.4°Cat760mmHg 
  • Flash Point:169°C 
  • Density:1.219g/cm3 
  • XLogP3:4.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:278.094294304
  • Heavy Atom Count:21
  • Complexity:335
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)COC(=O)OC2=CC3=CC=CC=C3C=C2
Technology Process of Benzyl naphthalen-2-yl carbonate

There total 1 articles about Benzyl naphthalen-2-yl carbonate 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 pyridine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/acs.orglett.8b02631
Guidance literature:
With methanol; sodium tetrahydroborate; nickel(II) chloride hexahydrate; at 20 ℃; for 0.25h; chemoselective reaction;
DOI:10.1007/s00706-018-2276-x
upstream raw materials:

benzyl chloroformate

β-naphthol

Downstream raw materials:

β-naphthol

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