Perhydropyrene

Perhydropyrene

IUPAC name Hexadecahydropyrene
Identifiers
CAS number	2435-85-0
PubChem	75524
ChemSpider	68050^Y
Jmol-3D images	Image 1
SMILES C2CCC3CCC1C4C(CCC1)CCC2C34
InChI InChI=1S/C16H26/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h11-16H,1-10H2^Y Key: BYBPEZLZCGOWIS-UHFFFAOYSA-N^Y InChI=1S/C16H26/c1-3-11-7-9-13-5-2-6-14-10-8-12(4-1)15(11)16(13)14/h11-16H,1-10H2
Properties
Molecular formula	C₁₆H₂₆
Molar mass	218.38 g mol⁻¹
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Perhydropyrene is a hydrocarbon similar to pyrene. Single bonds with hydrogen replace the double bonds in the benzene rings.

External links

Ayub, Khurshid; Zhang, Rui; Robinson, Stephen G.; Twamley, Brendan; Williams, Richard Vaughan; Mitchell, Reginald H. (2008). "Suppressing the Thermal Metacyclophanediene to Dihydropyrene Isomerization: Synthesis and Rearrangement of 8,16-Dicyano(2.2)metacyclophane-1,9-diene and Evidence Supporting the Proposed Biradicaloid Mechanism". The Journal of Organic Chemistry 73 (2): 451. doi:10.1021/jo7019459. PMID 18154301. http://pubs.acs.org/doi/abs/10.1021/jo7019459.
Mitchell, R (1996). "Synthesis of the elusive dibenzannelated dihydropyrene dibenzo(e,l)dimethyldihydropyrene, a molecular photo-switch". Tetrahedron Letters 37: 5239. doi:10.1016/0040-4039(96)01074-X. http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6THS-3Y0S3HR-24&_user=10&_coverDate=07%2F22%2F1996&_rdoc=1&_fmt=high&_orig=gateway&_origin=gateway&_sort=d&_docanchor=&view=c&_searchStrId=1708811652&_rerunOrigin=google&_acct=C000050221&_version=1&_urlVersion=0&_userid=10&md5=8510699b97fee8a258cec7f583cc9189&searchtype=a.