Misplaced Pages

Borirane: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editContent deleted Content addedVisualWikitext
Revision as of 05:57, 16 June 2020 editJérôme (talk | contribs)Extended confirmed users3,609 edits Period← Previous edit Latest revision as of 06:05, 5 November 2020 edit undoCitation bot (talk | contribs)Bots5,452,713 edits Alter: isbn, url. URLs might have been internationalized/anonymized. Add: author pars. 1-1. Removed parameters. Some additions/deletions were actually parameter name changes. Correct ISBN10 to ISBN13. | You can use this bot yourself. Report bugs here. | Suggested by AManWithNoPlan | All pages linked from cached copy of User:AManWithNoPlan/sandbox2 | via #UCB_webform_linked 1188/1577 
Line 37: Line 37:
'''Borirane''' is a ] ] with the ] ]<sub>2</sub>]<sub>4</sub>]H. This colourless, flammable gas is the simplest borirane, a three-membered ring consisting of two carbon and one boron atom. It can be viewed as a ] of ], with boron replacing the ] atom of aziridine. Borirane is ]ic with ]. '''Borirane''' is a ] ] with the ] ]<sub>2</sub>]<sub>4</sub>]H. This colourless, flammable gas is the simplest borirane, a three-membered ring consisting of two carbon and one boron atom. It can be viewed as a ] of ], with boron replacing the ] atom of aziridine. Borirane is ]ic with ].


This compound has five isomers.<ref>{{Cite book|title = Organometallic Chemistry|last = Stone|first = F. G. A.|publisher = Royal Society of Chemistry|year = 1987|isbn = |location = London|pages = 40|last2 = Abel|first2 = E. W.|url = https://books.google.com/books?id=LvvrQW1mKewC&pg=PA40&lpg=PA40&dq=Borirane+uses&source=bl&ots=uFGQFsjtMW&sig=qYy5n06L_5koWbidaC7pVpKGpGI&hl=en&sa=X&ved=0ahUKEwjpraKGtLfKAhWKqh4KHb7gBUMQ6AEIWzAK#v=onepage&q=Borirane%20uses&f=false|volume = 16}}</ref> This compound has five isomers.<ref>{{Cite book|title = Organometallic Chemistry|last1 = Stone|first1 = F. G. A.|publisher = Royal Society of Chemistry|year = 1987|isbn = 9780851866413|location = London|pages = 40|last2 = Abel|first2 = E. W.|url = https://books.google.com/books?id=LvvrQW1mKewC&q=Borirane+uses&pg=PA40|volume = 16}}</ref>


== References == == References ==

Latest revision as of 06:05, 5 November 2020

Borirane
Skeletal formula of borirane
Skeletal formula of borirane
Space-filling model of borirane
Space-filling model of borirane
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C2H5B/c1-2-3-1/h3H,1-2H2Key: OGVHYCXTHGZYKN-UHFFFAOYSA-N
  • InChI=1/C2H5B/c1-2-3-1/h3H,1-2H2
SMILES
  • B1CC1
Properties
Chemical formula BC
2H
5
Molar mass 39.872 g mol
Melting point −129 °C (−200 °F; 144 K)
Boiling point −24 °C (−11 °F; 249 K)
Solubility in water 15.425 g dm
Related compounds
Related heterocycles Aziridine
Ethylene oxide
Thiirane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Borirane is a heterocyclic organic compound with the formula C2H4BH. This colourless, flammable gas is the simplest borirane, a three-membered ring consisting of two carbon and one boron atom. It can be viewed as a structural analog of aziridine, with boron replacing the nitrogen atom of aziridine. Borirane is isomeric with ethylideneborane.

This compound has five isomers.

References

  1. Stone, F. G. A.; Abel, E. W. (1987). Organometallic Chemistry. Vol. 16. London: Royal Society of Chemistry. p. 40. ISBN 9780851866413.
Categories:
Borirane: Difference between revisions Add topic