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Naphthalene-1-13C

Base Information
  • Chemical Name:Naphthalene-1-13C
  • CAS No.:20526-83-4
  • Molecular Formula:C10H8
  • Molecular Weight:129.163
  • Hs Code.:
  • European Community (EC) Number:685-244-1
  • DSSTox Substance ID:DTXSID00480141
  • Nikkaji Number:J1.014.975D
  • Wikidata:Q82314714
  • Mol file:20526-83-4.mol
Naphthalene-1-13C

Synonyms:Naphthalene-1-13C;20526-83-4;DTXSID00480141;AKOS015913401;Naphthalene-1-13c,99 atom % 13c;Naphthalene-1-13C, 99 atom % 13C;J-013384

Suppliers and Price of Naphthalene-1-13C
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
  • Sigma-Aldrich
  • Naphthalene-1-13C 99 atom %
  • 10mg
  • $ 397.00
  • American Custom Chemicals Corporation
  • NAPHTHALENE-1-13C 95.00%
  • 10MG
  • $ 879.25
Total 1 raw suppliers
Chemical Property of Naphthalene-1-13C
Chemical Property:
  • Melting Point:80-82 °C(lit.)  
  • Boiling Point:218 °C(lit.)  
  • Flash Point:80℃ 
  • PSA:0.00000 
  • Density:1.037g/cm3 
  • LogP:2.83980 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:129.065955091
  • Heavy Atom Count:10
  • Complexity:80.6
Purity/Quality:

97% *data from raw suppliers

Naphthalene-1-13C 99 atom % *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xn,
  • Hazard Codes:Xn,N 
  • Statements: 22-40-50/53 
  • Safety Statements: 36/37-46-60-61 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C=CC=CC2=C1
  • Isomeric SMILES:C1=CC2=CC=C[13CH]=C2C=C1
Technology Process of Naphthalene-1-13C

There total 10 articles about Naphthalene-1-13C 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 5 steps
1: SOCl2 / CHCl3
2: tetrahydrofuran
3: LiAlH4, AlCl3 / diethyl ether
4: methanesulfonyl chloride, triethylamine / benzene / 10 °C
5: 900 °C / 0 Torr
With lithium aluminium tetrahydride; aluminium trichloride; thionyl chloride; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; diethyl ether; chloroform; benzene;
DOI:10.1021/ja00025a055
Guidance literature:
Multi-step reaction with 2 steps
1: methanesulfonyl chloride, triethylamine / benzene / 10 °C
2: 900 °C / 0 Torr
With methanesulfonyl chloride; triethylamine; In benzene;
DOI:10.1021/ja00025a055
Guidance literature:
Multi-step reaction with 4 steps
1: tetrahydrofuran
2: LiAlH4, AlCl3 / diethyl ether
3: methanesulfonyl chloride, triethylamine / benzene / 10 °C
4: 900 °C / 0 Torr
With lithium aluminium tetrahydride; aluminium trichloride; methanesulfonyl chloride; triethylamine; In tetrahydrofuran; diethyl ether; benzene;
DOI:10.1021/ja00025a055
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