Compound Identification
SMILES
CCOC(=O)C1=NN(C(=O)C2=C(NC(=O)C=CC)SC=C12)C1=CC=C(C)C=C1
InChIKey
InChIKey=GIIBXEVVEADBCT-UHFFFAOYSA-N
Formula
C20H19N3O4S
Mass
397.45
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Thienopyridazines
- Subclass Thieno[3,4-d]pyridazines
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Class
Thienopyridazines
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Thienopyridazines
Subclass
Thieno[3,4-d]pyridazines
Intermediate Tree Nodes
Not available
Direct Parent
Thieno[3,4-d]pyridazines
Alternative Parents
N-arylamides Toluenes Pyridazinones Vinylogous amides Thiophenes Heteroaromatic compounds Secondary carboxylic acid amides Lactams Carboxylic acid esters Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thieno[3,4-d]pyridazine - N-arylamide - Pyridazinone - Toluene - Monocyclic benzene moiety - Pyridazine - Benzenoid - Thiophene - Heteroaromatic compound - Vinylogous amide - Carboxamide group - Carboxylic acid ester - Lactam - Secondary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as thieno[3,4-d]pyridazines. These are organic heterocyclic compounds consisting of a thieno[3,4-d]pyridazine moiety. Thieno[3,4-d]pyridazine is a bicyclic compound made up of a thiophene ring fused to a pyridazine ring so that the sulfur atom and the two nitrogen atoms are at the 1-, 4-, and 5-position, respectively.
External Descriptors
Not available