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Polycyclic organic compounds, oakwoodchemical.com, aksci.com, www.tcichemicals.com


Cyclic compounds (2)
Aromatic compound (1)
Aromatic compounds (1)
Polycyclic aromatic compounds (1)
Tetracyclic compounds (1)


Matrix Scientific (2)
Sigma Aldrich (2)
Apollo Scientific (1)
Frontier Scientific (1)

1,1,1,2-TETRACHLOROETHANE (23425-39-0, 630-20-6)  
1,1,1,2-Tetrachloroethane is a chlorinated hydrocarbon. It is a colorless liquid with a sweet chloroform-like odor. It is used as a solvent and in the production of wood stains and varnishes.
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.
1,6-Dihydroxynaphthalene (575-44-0)  
FLUORANTHENE (206-44-0, 76774-50-0)  
Fluoranthene is a polycyclic aromatic hydrocarbon (PAH). The molecule can be viewed as the fusion of naphthalene and benzene unit connected by a five-membered ring. Although samples are often pale yellow, the compound is colorless.
Pentachloroethane is a non-flammable but toxic chemical compound of chlorine, hydrogen, and carbon. It is used as a solvent for oil and grease, in metal cleaning, and in the separation of coal from impurities.
4-Fluoronitrobenzene (350-46-9)  
o-fluoronitrobenzene  ·  p-fluoronitrobenzene  ·  2-fluoronitrobenzene
1,1,2,2-TETRABROMOETHANE (79-27-6)  
Tetrabromoethane (TBE) is a halogenated hydrocarbon, chemical formula C2H2Br4. Although three bromine atoms may bind to one of the carbon atoms creating 1,1,1,2-tetrabromoethane this is not thermodynamically favorable, so in practice tetrabromoethane is equal to 1,1,2,2-tetrabromoethane, where each carbon atom binds two bromine atoms. It has an unusually high density for an organic compound, near 3 g/mL, due largely to the four bromine atoms.
1,2,3,4-Tetraphenylnaphthalene (751-38-2)  
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.
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