Compound Identification
SMILES
[O-][N+](=O)C1=CC2=C(S\C(C=C2)=C(\C=O)C2=CC=CC=C2)C=C1
InChIKey
InChIKey=XSQHXGFTMYMKMT-ICFOKQHNSA-N
Formula
C17H11NO3S
Mass
309.34
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 Phenylacetaldehydes Aryl thioethers Nitroaromatic compounds Vinylogous thioesters Thiopyrans Enals Thioenol ethers Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Aldehydes Hydrocarbon derivatives Organic salts Organonitrogen compounds Organic oxides Organic cations
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
2h-thiochromene - 1-benzothiopyran - Benzothiopyran - Phenylacetaldehyde - Aryl thioether - Nitroaromatic compound - Monocyclic benzene moiety - Vinylogous thioester - Thiopyran - Benzenoid - Alpha,beta-unsaturated aldehyde - Enal - C-nitro compound - Organic nitro compound - Thioenolether - Organic oxoazanium - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic salt - Organooxygen compound - Organonitrogen compound - Aldehyde - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic nitrogen compound - Organic oxygen 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