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Benzothiazole, 2-[[(trimethylsilyl)methyl]thio]-

Base Information Edit
  • Chemical Name:Benzothiazole, 2-[[(trimethylsilyl)methyl]thio]-
  • CAS No.:106296-62-2
  • Molecular Formula:C11H15NS2Si
  • Molecular Weight:253.464
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70395915
  • Nikkaji Number:J1.970.823C
  • Wikidata:Q82196300
  • Mol file:106296-62-2.mol
Benzothiazole, 2-[[(trimethylsilyl)methyl]thio]-

Synonyms:Benzothiazole, 2-[[(trimethylsilyl)methyl]thio]-;106296-62-2;2-{[(trimethylsilyl)methyl]sulfanyl}-1,3-benzothiazole;DTXSID70395915;2-[[(Trimethylsilyl)methyl]thio]benzothiazole;InChI=1/C11H15NS2Si/c1-15(2,3)8-13-11-12-9-6-4-5-7-10(9)14-11/h4-7H,8H2,1-3H

Suppliers and Price of Benzothiazole, 2-[[(trimethylsilyl)methyl]thio]-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of Benzothiazole, 2-[[(trimethylsilyl)methyl]thio]- Edit
Chemical Property:
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:3
  • Exact Mass:253.04151836
  • Heavy Atom Count:15
  • Complexity:217
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C[Si](C)(C)CSC1=NC2=CC=CC=C2S1
Technology Process of Benzothiazole, 2-[[(trimethylsilyl)methyl]thio]-

There total 2 articles about Benzothiazole, 2-[[(trimethylsilyl)methyl]thio]- 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 lithium diisopropyl amide; Yield given. Multistep reaction; 1.) THF, -78 deg C, 1 h; 2.) THF, -78 deg C, 4 h;
Guidance literature:
With lithium diisopropyl amide; Yield given. Multistep reaction; 1.) THF, -78 deg C, 1 h; 2.) THF, -78 deg C, 4 h;
Guidance literature:
With tris(dimethylamino)sulfonium trimethylsilyldifluoride; In tetrahydrofuran; for 3h; Ambient temperature;
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