| Weight | 347.661 g/mol |
|---|---|
| Formula | Cl6N3P3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Phosphonitrilic chloride trimer (9047-50-1, 940-71-6)
hexachlorocyclotriphosphazene · hexachlorocyclotriphosphazene, radical ion (1-) · hexachlorocyclotriphosphazene, 1,3,5-(15)N3-labeled
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- Phosphonitrilic Compounds. V. Cyclized Products from the Reactions of Hexachlorocyclotriphosphazene (Phosphonitrilic Chloride Trimer) with Aromatic Dihydroxy, Dithiol, and Diamino Compounds (Inorganic Chemistry, 1966)
- Polymerization of Hexachlorocyclotriphosphazene. The Role of Phosphorus Pentachloride, Water, and Hydrogen Chloride (Macromolecules, 1975)
- Competitive formation of spiro and ansa derivatives in the reactions of tetrafluorobutane-1,4-diol with hexachlorocyclotriphosphazene: a comparison with butane-1,4-diol (Polyhedron, 2006)
- Phosphorus-nitrogen compounds. XXIII. Reaction of sodium 2,2,2-trifluoroethoxide with hexachlorocyclotriphosphazene (Inorganic Chemistry, 1975)
- Kinetics and mechanism of the boron trichloride catalyzed thermal ring-opening polymerization of hexachlorocyclotriphosphazene in 1,2,4-trichlorobenzene solution (Macromolecules, 1986)
- New Reactions of Phosphonitrilic Chloride Trimer. Substitution and Cleavage Reactions with Catechol and Triethylamine (Journal of the American Chemical Society, 1963)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - hexachlorocyclotriphosphazene
- hexachlorocyclotriphosphazene, radical ion (1-)
- hexachlorocyclotriphosphazene, 1,3,5-(15)N3-labeled
-
SMILESN1=P(N=P(N=P1(Cl)Cl)(Cl)Cl)(Cl)Cl
-
InChIKeyUBIJTWDKTYCPMQ-UHFFFAOYSA-N
- Pubchem - Phosphonitrilic chloride trimer
- Wikipedia - hexachlorocyclotriphosphatriazene
Hexachlorophosphazene is an inorganic compound with the formula (NPCl2)3. The molecule has a cyclic backbone consisting of alternating phosphorus and nitrogen atoms. It can be viewed as a trimer of the hypothetical compound NPCl2.
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