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anguibactin

Base Information
  • Chemical Name:anguibactin
  • CAS No.:104245-09-2
  • Molecular Formula:C15H16N4O4S
  • Molecular Weight:348.382
  • Hs Code.:
anguibactin

Synonyms:anguibactin

Suppliers and Price of anguibactin
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
  • American Custom Chemicals Corporation
  • ANGUIBACTIN 95.00%
  • 5MG
  • $ 496.69
Total 3 raw suppliers
Chemical Property of anguibactin
Chemical Property:
  • Vapor Pressure:1.07E-24mmHg at 25°C 
  • Boiling Point:766.4°Cat760mmHg 
  • Flash Point:417.3°C 
  • PSA:143.85000 
  • Density:1.609g/cm3 
  • LogP:0.99620 
Purity/Quality:

95% *data from raw suppliers

ANGUIBACTIN 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of anguibactin

There total 5 articles about anguibactin 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:

Reference yield: 88.0%

Guidance literature:
With boron trichloride; tetra-(n-butyl)ammonium iodide; In dichloromethane; at -78 ℃; for 2h; Inert atmosphere;
DOI:10.1021/acs.orglett.8b02789
Guidance literature:
Multi-step reaction with 2 steps
1: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 4 h / 20 °C / Inert atmosphere
2: tetra-(n-butyl)ammonium iodide; boron trichloride / dichloromethane / 2 h / -78 °C / Inert atmosphere
With boron trichloride; tetra-(n-butyl)ammonium iodide; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In dichloromethane;
DOI:10.1021/acs.orglett.8b02789
Guidance literature:
Multi-step reaction with 3 steps
1: aq. phosphate buffer; methanol / 24 h / 50 °C / pH 6.4 / Inert atmosphere
2: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / dichloromethane / 4 h / 20 °C / Inert atmosphere
3: tetra-(n-butyl)ammonium iodide; boron trichloride / dichloromethane / 2 h / -78 °C / Inert atmosphere
With boron trichloride; tetra-(n-butyl)ammonium iodide; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In methanol; aq. phosphate buffer; dichloromethane;
DOI:10.1021/acs.orglett.8b02789
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