Bicyclo(2.2.1)heptane-2-carbonitrile

Bicyclo[2.2.1]heptane-2-carbonitrile
Names
	IUPAC name Bicyclo[2.2.1]heptane-2-carbonitrile
	Other names 2-Norbornanecarbonitrile
Identifiers
CAS Number	2234-26-6 ; 3211-87-8 (endo) ; 3211-90-3 (exo) ;
3D model (JSmol)	Interactive image;
ChemSpider	92361;
ECHA InfoCard	100.017.076
PubChem CID	102231;
UNII	57U33ASF4X ;
CompTox Dashboard (EPA)	DTXSID90870431 DTXSID20870949, DTXSID90870431 ;
	InChI InChI=1S/C8H11N/c9-5-8-4-6-1-2-7(8)3-6/h6-8H,1-4H2 Key: GAHKEUUHTHVKEA-UHFFFAOYSA-N; InChI=1/C8H11N/c9-5-8-4-6-1-2-7(8)3-6/h6-8H,1-4H2 Key: GAHKEUUHTHVKEA-UHFFFAOYAS;
	SMILES N#CC2CC1CCC2C1;
Properties
Chemical formula	C8H11N
Molar mass	121.183 g·mol−1
Melting point	43 to 45 °C (109 to 113 °F; 316 to 318 K) 10 mmHg
Boiling point	73 to 75 °C (163 to 167 °F; 346 to 348 K)10 mmHg
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Bicyclo[2.2.1]heptane-2-carbonitrile is a chemical which is classified as an extremely hazardous substance in the United States. It is defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.^[2]

References

^ ^a ^b 2-Norbornanecarbonitrile at Sigma-Aldrich
^ "40 C.F.R.: Appendix A to Part 355—The List of Extremely Hazardous Substances and Their Threshold Planning Quantities" (PDF). Code of Federal Regulations (July 1, 2008 ed.). Government Printing Office. Archived from the original (PDF) on February 25, 2012. Retrieved October 29, 2011.

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

[Aldrich-1] 2-Norbornanecarbonitrile at Sigma-Aldrich

[gov-right-know-2] "40 C.F.R.: Appendix A to Part 355—The List of Extremely Hazardous Substances and Their Threshold Planning Quantities" (PDF). Code of Federal Regulations (July 1, 2008 ed.). Government Printing Office. Archived from the original (PDF) on February 25, 2012. Retrieved October 29, 2011.

[1]

[2]

See also

References