CC1(C)[C@@H]2CC[C@@]1(CS(=O)(=O)N(C1CCCCC1)C1CCCCC1)[C@@H](C2)O[C@@H]1C[C@H](C2=CC=C(Cl)C=C2)C(C#N)=[N+]([O-])O1

InChIKey=ZAXIFQXESOLQEI-PHAPKVCRSA-N

C33H46ClN3O5S

632.26

Organic compounds

Lipids and lipid-like molecules

Prenol lipids

Monoterpenoids

Not available

Bicyclic monoterpenoids

Aromatic monoterpenoids Chlorobenzenes Organosulfonamides Organic sulfonamides Aryl chlorides Aminosulfonyl compounds Oxacyclic compounds Allyl-type 1,3-dipolar organic compounds Azacyclic compounds Nitriles Organopnictogen compounds Hydrocarbon derivatives Organic oxides Organic salts Organochlorides Organooxygen compounds Organic cations

Aromatic heteropolycyclic compounds

Aromatic monoterpenoid - Bornane monoterpenoid - Bicyclic monoterpenoid - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Organic sulfonic acid amide - Organosulfonic acid amide - Benzenoid - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Oxacycle - Azacycle - Carbonitrile - Nitrile - Organoheterocyclic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organochloride - Organohalogen compound - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Cyanide - Organic salt - Organic oxide - Hydrocarbon derivative - Organic cation - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.

Not available