Phosphirane

Phosphirane
Names
	Preferred IUPAC name Phosphirane
	Systematic IUPAC name Phosphacyclopropane
	Other names Phosphiran
Identifiers
CAS Number	6569-82-0;
3D model (JSmol)	Interactive image;
ChemSpider	10451470;
PubChem CID	15786916;
	InChI InChI=1S/C2H5P/c1-2-3-1/h3H,1-2H2 Key: UTMQOVWWMLZKRY-UHFFFAOYSA-N;
	SMILES C1PC1;
Properties
Chemical formula	C2H5P
Molar mass	60.036 g·mol−1
Appearance	colorless gas
Melting point	−121 °C (−186 °F; 152 K)
Boiling point	36.5 °C (97.7 °F; 309.6 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Phosphirane is the organophosphorus compound with the formula C₂H₄PH. It is a colorless gas of no commercial value. As the simplest cyclic, saturated organophosphorus compound, phosphirane is the prototype of a family of related compounds that have attracted attention from the research community. Phosphirane was first prepared by reaction of 1,2-dichloroethane with the conjugate base of phosphine.^[2] Phosphiranes, that is substituted phosphirene compounds where one or more of the H's are replaced organic substituents, are far more commonly discussed than the parent phosphirane.

References[]

^ Wagner, Ross I.; Freeman, LeVern D.; Goldwhite, H.; Rowsell, D. G. (March 1967). "Phosphiran". Journal of the American Chemical Society. 89 (5): 1102–1104. doi:10.1021/ja00981a013.
^ François Mathey, Manfred Regitz (1996). "Phosphiranes, Phosphirenes, and Heavier Analogues". Comprehensive Heterocyclic Chemistry II. 1A. pp. 277–304. doi:10.1016/B978-008096518-5.00008-3.CS1 maint: uses authors parameter (link)

Quin, L. D. (2000). A Guide to Organophosphorus Chemistry. Wiley-Interscience. ISBN 0-471-31824-8.

[1] Wagner, Ross I.; Freeman, LeVern D.; Goldwhite, H.; Rowsell, D. G. (March 1967). "Phosphiran". Journal of the American Chemical Society. 89 (5): 1102–1104. doi:10.1021/ja00981a013.

[2] François Mathey, Manfred Regitz (1996). "Phosphiranes, Phosphirenes, and Heavier Analogues". Comprehensive Heterocyclic Chemistry II. 1A. pp. 277–304. doi:10.1016/B978-008096518-5.00008-3.CS1 maint: uses authors parameter (link)

[1]

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