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Urea, N-2H-1,4-benzothiazin-3-yl-N'-phenyl-

Base Information Edit
  • Chemical Name:Urea, N-2H-1,4-benzothiazin-3-yl-N'-phenyl-
  • CAS No.:108176-66-5
  • Molecular Formula:C15H13N3OS
  • Molecular Weight:283.354
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40148455
  • Wikidata:Q83013988
  • Mol file:108176-66-5.mol
Urea, N-2H-1,4-benzothiazin-3-yl-N'-phenyl-

Synonyms:BRN 5580657;Urea, N-2H-1,4-benzothiazin-3-yl-N'-phenyl-;N-2H-1,4-Benzothiazin-3-yl-N'-phenylurea;108176-66-5;DTXSID40148455;LS-158899

Suppliers and Price of Urea, N-2H-1,4-benzothiazin-3-yl-N'-phenyl-
Supply Marketing:Edit
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 4 raw suppliers
Chemical Property of Urea, N-2H-1,4-benzothiazin-3-yl-N'-phenyl- Edit
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:1.32g/cm3 
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:283.07793322
  • Heavy Atom Count:20
  • Complexity:379
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(=NC2=CC=CC=C2S1)NC(=O)NC3=CC=CC=C3
Technology Process of Urea, N-2H-1,4-benzothiazin-3-yl-N'-phenyl-

There total 3 articles about Urea, N-2H-1,4-benzothiazin-3-yl-N'-phenyl- 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 2 steps
1: 5 percent ethanolic HCl / 2 h / Heating
2: 61 percent / toluene / Heating
With hydrogenchloride; In toluene;
Guidance literature:
Multi-step reaction with 3 steps
1: 25 percent aq. NaOH, tetrabutylammonium hydrogen sulphate / CH2Cl2 / 4 h / Ambient temperature
2: 5 percent ethanolic HCl / 2 h / Heating
3: 61 percent / toluene / Heating
With hydrogenchloride; sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate; In dichloromethane; toluene;
Refernces Edit
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