Polycyclic organic compounds, Cyclopentenes, Antiparkinsonian agents, Drugs acting on the nervous system
Cyclic compounds (1)
1,2,3,4-Tetraphenylnaphthalene is a polycyclic aromatic hydrocarbon commonly prepared in the undergraduate teaching laboratory as an introduction to the Diels-Alder reaction, in this case between benzyne, which acts as the dienophile, (generated in situ) and tetraphenylcyclopentadienone, which acts as the diene. It has two crystalline forms, and therefore has two different melting points.
1-METHYLNAPHTHALENE (90-12-0, 1321-94-4)
1-Methylnaphthalene is a polycyclic aromatic hydrocarbon (PAH). It has a cetane number of zero, and was previously used as the lower reference for cetane number. However, due to the expense and handling difficulty of 1-methylnaphthalene, it was replaced in this capacity by isocetane, with a CN of 15.
2,6-DIPN · 2,6-disopropylnaphtalene
2,6-Diisopropylnaphthalene (2,6-DIPN) is structurally similar to other plant growth regulators commonly found in plant tissues, and seems to help inhibit the sprouting of potatoes during storage. 2,6-DIPN is intended for use in the manufacturing of pesticide products intended to prevent sprouting of stored potatoes.
FLUORENE (2299-68-5, 86-73-7)
Fluorene , or 9H-fluorene, is a polycyclic aromatic hydrocarbon. It forms white crystals that exhibit a characteristic, aromatic odor similar to that of naphthalene. It is combustible.
naphthalene (91-20-3, 68412-25-9)
Naphthalene is an organic compound with formula C 10H 8. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass. As an aromatic hydrocarbon, naphthalene's structure consists of a fused pair of benzene rings.