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TETRAFLUOROPYRIDAZINE

Base Information
  • Chemical Name:TETRAFLUOROPYRIDAZINE
  • CAS No.:7627-80-7
  • Molecular Formula:C4F4N2
  • Molecular Weight:152.051
  • Hs Code.:
  • Mol file:7627-80-7.mol
TETRAFLUOROPYRIDAZINE

Synonyms:3,4,5,6-Tetrafluorpyridazin;Pyridazine,tetrafluoro;Tetrafluorpyrazin;Tetrafluor-pyridazin;Tetrafluorpyrydazin;tetrafluoro-pyridazine;perfluoropyridazine;

Suppliers and Price of TETRAFLUOROPYRIDAZINE
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
  • SynChem
  • TETRAFLUOROPYRIDAZINE 95%
  • 1 g
  • $ 250.00
  • CHESS?
  • SG000657:3,4,5,6-Tetrafluoro-pyridazine 98
  • 1 g
  • $ 180.00
  • American Custom Chemicals Corporation
  • TETRAFLUOROPYRIDAZINE 98.00%
  • 10G
  • $ 1715.18
  • Alfa Aesar
  • Tetrafluoropyridazine 97%
  • 500mg
  • $ 291.49
Total 10 raw suppliers
Chemical Property of TETRAFLUOROPYRIDAZINE
Chemical Property:
  • Vapor Pressure:0.485mmHg at 25°C 
  • Boiling Point:199.3°C at 760 mmHg 
  • Flash Point:74.3°C 
  • PSA:25.78000 
  • Density:1.639g/cm3 
  • LogP:1.03300 
Purity/Quality:

97% *data from raw suppliers

TETRAFLUOROPYRIDAZINE 95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • General Description Tetrafluoropyridazine is a highly fluorinated heterocyclic compound that serves as a versatile precursor for synthesizing complex polyfunctional heterocyclic systems, such as tricyclic 9,10-dioxa-1,2-diaza-anthracene derivatives. Its reactivity in nucleophilic aromatic substitution reactions enables efficient ring annelation processes, making it valuable for constructing rare heterocyclic scaffolds with potential applications in drug discovery and materials chemistry.
Refernces

9,10-Dioxa-1,2-diaza-anthracene derivatives from tetrafluoropyridazine

10.3762/bjoc.6.45

The research explores the synthesis of a tricyclic 9,10-dioxa-1,2-diaza-anthracene system from tetrafluoropyridazine and catechol through a sequential nucleophilic aromatic substitution ring annelation process. The purpose of this study is to further utilize perfluoroheteroaromatic derivatives for the creation of unusual polyfunctional heterocyclic architectures, which could be valuable in drug discovery programs. The researchers successfully synthesized the tricyclic scaffold and reacted it with various nucleophiles, including amines and sodium ethoxide, to produce a series of functional 9,10-dioxa-1,2-diaza-anthracene systems. The study concludes that a small range of dioxa-1,2-diaza-anthracene analogues can be efficiently synthesized from tetrafluoropyridazine in two steps, expanding the application of highly fluorinated heterocycles for the synthesis of rare heterocyclic architectures.

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