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4-Butylsulfanylquinazoline

Base Information
  • Chemical Name:4-Butylsulfanylquinazoline
  • CAS No.:6956-61-2
  • Molecular Formula:C12H14N2S
  • Molecular Weight:218.323
  • Hs Code.:
  • NSC Number:65058
  • DSSTox Substance ID:DTXSID40289877
  • Nikkaji Number:J1.468.596K
  • Wikidata:Q82027395
4-Butylsulfanylquinazoline

Synonyms:4-butylsulfanylquinazoline;6956-61-2;4-(butylthio)quinazoline;NSC 65058;4-Butylthioquinazoline;NSC65058;SCHEMBL5136561;DTXSID40289877;NSC-65058;AKOS017144608;A842035

Suppliers and Price of 4-Butylsulfanylquinazoline
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
Total 6 raw suppliers
Chemical Property of 4-Butylsulfanylquinazoline
Chemical Property:
  • Vapor Pressure:4.84E-05mmHg at 25°C 
  • Boiling Point:359.7°Cat760mmHg 
  • Flash Point:171.3°C 
  • Density:1.15g/cm3 
  • XLogP3:3.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:4
  • Exact Mass:218.08776963
  • Heavy Atom Count:15
  • Complexity:187
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCSC1=NC=NC2=CC=CC=C21
Technology Process of 4-Butylsulfanylquinazoline

There total 3 articles about 4-Butylsulfanylquinazoline 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 potassium hydroxide; tetrabutylammomium bromide; In cyclohexane; Heating;
DOI:10.1016/S0014-827X(00)00100-2
Guidance literature:
Multi-step reaction with 3 steps
1: 47 percent / 4 h / 120 - 125 °C
2: 93 percent / P4S10; pyridine / 20 h / Heating
3: 80 percent / tetrabutylammonium bromide; KOH / cyclohexane / Heating
With pyridine; potassium hydroxide; tetraphosphorus decasulfide; tetrabutylammomium bromide; In cyclohexane;
DOI:10.1016/S0014-827X(00)00100-2
Guidance literature:
Multi-step reaction with 2 steps
1: 93 percent / P4S10; pyridine / 20 h / Heating
2: 80 percent / tetrabutylammonium bromide; KOH / cyclohexane / Heating
With pyridine; potassium hydroxide; tetraphosphorus decasulfide; tetrabutylammomium bromide; In cyclohexane;
DOI:10.1016/S0014-827X(00)00100-2
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