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Polycyclic organic compounds, matrixscientific.com, Heterocyclic compounds (4 or more rings), www.sigmaaldrich.com

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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.
1,2,3,4-Tetrahydronaphthalene (68412-24-8, 119-64-2)  
tetralin
Tetralin (1,2,3,4-tetrahydronaphthalene) is a hydrocarbon having the chemical formula C10H12. This molecule is similar to the naphthalene chemical structure except that one ring is saturated.
1-Fluoro-2-nitrobenzene (1493-27-2)  
o-fluoronitrobenzene  ·  p-fluoronitrobenzene  ·  2-fluoronitrobenzene
FLUORENE (2299-68-5, 86-73-7)  
9H-fluorene
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.
rosefuran (15186-51-3)  
Rosefuran (3-methyl-2-prenylfuran) is a liquid boiling at 103-104 °C (at 50 mm Hg), with a density of 0.9089 g/cm3 (at 30 °C), less than that of water. It is an aroma chemical which is a minor constituent of the aroma of the rose (Rosa damascene). Rosefuran is a 2,3-disubstituted furan (3-methyl-2-(3-methyl-2-buten-1-yl)furan).
Perillen (539-52-6)  
Perillene is a natural monoterpene that consists of a furan ring with a six-carbon homoprenyl side chain. Perillene is a component of the essential oil obtained by extraction of the leaves of Perilla frutescens. Perillene has also been obtained by steam distillation of the leaves of Perilla frutescens.
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