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Benzothiazole, 2,2'-ethylenebis-

Base Information
  • Chemical Name:Benzothiazole, 2,2'-ethylenebis-
  • CAS No.:965-16-2
  • Molecular Formula:C16H12N2S2
  • Molecular Weight:296.417
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70242278
  • Nikkaji Number:J41.954K
  • Wikidata:Q83125915
Benzothiazole, 2,2'-ethylenebis-

Synonyms:BENZOTHIAZOLE, 2,2'-ETHYLENEBIS-;2,2'-Ethylenebisbenzothiazole;965-16-2;2,2'-Dibenzothiazole-ethane;BRN 0258453;1,2-bis(benzo[d]thiazol-2-yl)ethane;2-[2-(1,3-benzothiazol-2-yl)ethyl]-1,3-benzothiazole;4-27-00-08491 (Beilstein Handbook Reference);C16H12N2S2;TimTec1_006854;SCHEMBL19372016;DTXSID70242278;HMS1553H12;STK874211;AKOS000547102;LS-40757;MLS-0067003.P001;Benzothiazole, 2,2'-(1,2-ethanediyl)bis-;EU-0039725;2,2'-ethane-1,2-diylbis(1,3-benzothiazole);SR-01000446443;SR-01000446443-1;BRD-K05762563-001-02-0

Suppliers and Price of Benzothiazole, 2,2'-ethylenebis-
Supply Marketing:
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Benzothiazole, 2,2'-ethylenebis-
Chemical Property:
  • XLogP3:5.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:3
  • Exact Mass:296.04419074
  • Heavy Atom Count:20
  • Complexity:306
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)N=C(S2)CCC3=NC4=CC=CC=C4S3
Technology Process of Benzothiazole, 2,2'-ethylenebis-

There total 2 articles about Benzothiazole, 2,2'-ethylenebis- 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:
In tetrahydrofuran; diethyl ether; under N2, addn. of soln. oftriphenylstannyliodide in THF to soln. of 2-(lithiomethyl)benzothiazole in Et2O, stirring at -78 ° C for 1 h, warming up to room temp.; evapn., residue redissolved in cyclohexane/ethyl acetate (1:3), washing with water, organic layer dried over MgSO4, major products are Ph3SnSnPh3 and 1,2-dibenzothiazolylethane;
DOI:10.1016/0022-328X(89)87167-0
Guidance literature:
In tetrahydrofuran; diethyl ether; under N2, addn. of a soln. of 2-lithiobenzothiazole in Et2O to soln. of triphenylstannylmethyliodide in THF, stirring at -78 ° C for 1 h, warming up to room temp.; evapn. resdue redissolved in cyclohexane/ethyl acetate (1:3), washing with water, organic layer dried over MgSO4, solvent removal, crystn. of Ph3Sn2Ph3 from petroleum ether;
DOI:10.1016/0022-328X(89)87167-0
Guidance literature:
beim Schmelzen;
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