OC1=C2O[C@H]3C4=C(C[C@@]5(O)[C@H]6CC(C=C1)=C2[C@@]35CCN6CC1CC1)C=C(C=N4)C1=C(Cl)C(Cl)=C(Cl)C=C1

InChIKey=BZLWVFHRAJLGRK-QYHPOFIQSA-N

C29H25Cl3N2O3

555.88

Organic compounds

Alkaloids and derivatives

Morphinans

Not available

Not available

Morphinans

Phenylquinolines Phenanthrenes and derivatives Phenylpyridines Tetralins Coumarans 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Aralkylamines Chlorobenzenes Piperidines Aryl chlorides Tertiary alcohols Heteroaromatic compounds Trialkylamines 1,2-aminoalcohols Oxacyclic compounds Azacyclic compounds Organochlorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Morphinan - Phenylquinoline - Phenanthrene - 3-phenylpyridine - Quinoline - Tetralin - Coumaran - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Halobenzene - Chlorobenzene - Aralkylamine - Piperidine - Aryl halide - Benzenoid - Aryl chloride - Pyridine - Monocyclic benzene moiety - Heteroaromatic compound - Tertiary alcohol - Tertiary aliphatic amine - Tertiary amine - 1,2-aminoalcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Ether - Amine - Organic oxygen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organohalogen compound - Organochloride - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as morphinans. These are polycyclic compounds with a four-ring skeleton with three condensed six-member rings forming a partially hydrogenated phenanthrene moiety, one of which is aromatic while the two others are alicyclic.

Not available