Compound Identification
SMILES
[O-][N+](=O)C1=C(NCCCN2CCOCC2)C2=CC=CC=C2SC1=O
InChIKey
InChIKey=NSIQIJLQSLVHDB-UHFFFAOYSA-N
Formula
C16H19N3O4S
Mass
349.41
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 Nitroaromatic compounds Secondary alkylarylamines Benzenoids Morpholines Vinylogous amides Carbothioic S-lactones Heteroaromatic compounds Trialkylamines Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Oxacyclic compounds Dialkyl ethers Organic oxoazanium compounds Organic salts Hydrocarbon derivatives Organic zwitterions Organic oxides
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thiochromene - 1-benzothiopyran - Benzothiopyran - Nitroaromatic compound - Secondary aliphatic/aromatic amine - Morpholine - Oxazinane - Benzenoid - Heteroaromatic compound - Vinylogous amide - Carbothioic s-lactone - C-nitro compound - Tertiary amine - Organic nitro compound - Tertiary aliphatic amine - Dialkyl ether - Ether - Organic oxoazanium - Secondary amine - Oxacycle - Azacycle - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Organic oxygen compound - Organic salt - Organic zwitterion - Amine - Organonitrogen compound - Organooxygen compound - 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