Compound Identification
SMILES
[O-][N+](=O)C1=CC=CC(=C1)C1C2=C(OC3=C1C(=O)SC1=CC=CC=C31)C1=CC=CC=C1C2=O
InChIKey
InChIKey=OCIWYBLEVUIZHU-UHFFFAOYSA-N
Formula
C25H13NO5S
Mass
439.44
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
- Class Thiochromenes
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Thiochromenes
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Thiochromenes
Alternative Parents
1-benzothiopyrans Indenes and isoindenes Nitrobenzenes Aryl ketones Nitroaromatic compounds Vinylogous esters Carbothioic S-lactones Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organic oxoazanium compounds Organopnictogen compounds Hydrocarbon derivatives Organic oxides Organic salts Organonitrogen compounds Aldehydes Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thiochromene - Indene - 1-benzothiopyran - Benzothiopyran - Nitrobenzene - Nitroaromatic compound - Aryl ketone - Monocyclic benzene moiety - Benzenoid - Heteroaromatic compound - Vinylogous ester - Carbothioic s-lactone - Ketone - C-nitro compound - Organic nitro compound - Organic oxoazanium - Oxacycle - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organooxygen compound - Organonitrogen compound - Aldehyde - Hydrocarbon derivative - Organic oxide - Organic salt - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic cation - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as thiochromenes. These are organosulfur compounds that are analogues to chromene, with the difference that a sulfur atom replaces the oxygen atom.
External Descriptors
Not available