Bornan

Bornan
Skeletal formula	Ball-and-stick model
	(1S,4S)-1,7,7-trimetilbiciklo[2.2.1]heptan
Identifikacija
PubChem	92108
Jmol-3D slike	Slika 1
SMILES
	CC1(C2CCC1(CC2)C)C
InChI
	InChI=1S/C10H18/c1-9(2)8-4-6-10(9,3)7-5-8/h8H,4-7H2,1-3H3 ; Kod: BEWYHVAWEKZDPP-UHFFFAOYSA-N
Svojstva
Molekulska formula	C10H18
Molarna masa	138.24992
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

Bornan (kamfan) je jedinjenje koje je blisko srodno sa norbornanima.^[3]

Biosinteza

Bornan se formira tokom biosinteze kamfora iz geranil pirofosfata, putem ciklizacije linaloil pirofosfata do bornil pirofosfata.^[4]

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Clayden Jonathan, Nick Greeves, Stuart Warren, Peter Wothers (2001). Organic chemistry. Oxford, Oxfordshire: Oxford University Press. ISBN 0-19-850346-6.
↑ Rodney Croteau, Frank Karp (1979). „Biosynthesis of monoterpenes: Hydrolysis of bornyl pyrophosphate, an essential step in camphor biosynthesis, and hydrolysis of geranyl pyrophosphate, the acyclic precursor of camphor, by enzymes from sage (Salvia officinalis)”. Archives of Biochemistry and Biophysics 198 (2): 523–532.