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Polycyclic organic compounds, Cyclopentanes, Bicyclic compounds

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(+)-Isothujone (471-15-8)  
Thujone ( ( listen)) is a ketone and a monoterpene that occurs naturally in two diastereomeric forms: (−)-α-thujone and (+)-β-thujone. It has a menthol odor. Though it is best known as a chemical compound in the spirit absinthe, which contains only small quantities of thujone, it is unlikely to be responsible for absinthe's alleged psychedelic effects.
Isothujone (471-15-8)  
Thujone ( ( listen)) is a ketone and a monoterpene that occurs naturally in two diastereomeric forms: (−)-α-thujone and (+)-β-thujone. It has a menthol odor. Though it is best known as a chemical compound in the spirit absinthe, which contains only small quantities of thujone, it is unlikely to be responsible for absinthe's alleged psychedelic effects.
3-Thujanone (546-80-5, 1125-12-8)  
thujone  ·  beta-thujone, 1S-(1alpha,4beta,5alpha)-isomer  ·  alpha-thujone
Thujone ( ( listen)) is a ketone and a monoterpene that occurs naturally in two diastereomeric forms: (−)-α-thujone and (+)-β-thujone. It has a menthol odor. Though it is best known as a chemical compound in the spirit absinthe, which contains only small quantities of thujone, it is unlikely to be responsible for absinthe's alleged psychedelic effects.
alpha-Thujone (546-80-5, 59573-80-7)  
thujone  ·  beta-thujone, 1S-(1alpha,4beta,5alpha)-isomer  ·  3-isothujone
Thujone ( ( listen)) is a ketone and a monoterpene that occurs naturally in two diastereomeric forms: (−)-α-thujone and (+)-β-thujone. It has a menthol odor. Though it is best known as a chemical compound in the spirit absinthe, which contains only small quantities of thujone, it is unlikely to be responsible for absinthe's alleged psychedelic effects.
CAMPHENE (79-92-5, 565-00-4, 5794-04-7)  
Camphene is a bicyclic monoterpene. It is nearly insoluble in water, but very soluble in common organic solvents. It volatilizes readily at room temperature and has a pungent smell.
(-)-Borneol (464-45-9, 507-70-0)  
borneol  ·  isoborneol  ·  isoborneol, (1R-endo)-isomer
L(-)-Borneol (507-70-0)  
borneol  ·  isoborneol  ·  isoborneol, (1R-endo)-isomer
Borneol is a bicyclic organic compound and a terpene derivative. The hydroxyl group in this compound is placed in an endo position. There are two different enantiomers of borneol.
Borneol (124-76-5, 464-43-7, 10385-78-1, 507-70-0)  
isoborneol  ·  isoborneol, (1R-endo)-isomer  ·  isoborneol, (1S-endo)-isomer
Borneol is a bicyclic organic compound and a terpene derivative. The hydroxyl group in this compound is placed in an endo position. There are two different enantiomers of borneol.
Isoborneol (10334-13-1, 124-76-5, 507-70-0)  
borneol  ·  isoborneol, (1R-endo)-isomer  ·  isoborneol, (1S-endo)-isomer
NORBORNANE (279-23-2)  
bicyclo(2.2.1)heptene  ·  b(2.2.1)heptene  ·  bicyclo(2.2.1)heptane
Norbornane (also known as bicyclo[2.2.1]heptane) is an organic compound and a saturated hydrocarbon with chemical formula C7H12. It is a crystalline compound with melting point 88 °C. The carbon skeleton is derived from cyclohexane ring with a methylene bridge in the 1,4- position, and is a bridged bicyclic compound.

Related Results:
2-METHYLNAPHTHALENE (7419-61-6, 91-57-6)  
2-methylnaphthalene, methyl-13C-labeled  ·  2-methylnaphthalene, lithium salt, ion(1-)  ·  2-methylnaphthalene, naphthalene-1-(13)C-labeled
2-Methylnaphthalene is a polycyclic aromatic hydrocarbon (PAH). On February 22, 2014, NASA announced a greatly upgraded database for detecting and monitoring PAHs, including 2-methylnaphthalene, in the universe. According to NASA scientists, over 20% of the carbon in the universe may be associated with PAHs, possible starting materials for the formation of life.
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.
Related searches
Polycyclic organic compounds
Cyclopentanes
Bicyclic compounds
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