Compound Identification
SMILES
CCC(=O)C1=NN(C(=O)C2=C(N)SC=C12)C1=C(C)C=C(C)C=C1
InChIKey
InChIKey=MQZFFFSXEIILDO-UHFFFAOYSA-N
Formula
C17H17N3O2S
Mass
327.4
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
m-Xylenes Aryl alkyl ketones Pyridazinones 2-aminothiophenes Vinylogous amides Heteroaromatic compounds Lactams Azacyclic compounds Primary amines Organic oxides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Thieno[3,4-d]pyridazine - M-xylene - Xylene - Aryl ketone - Aryl alkyl ketone - Pyridazinone - Monocyclic benzene moiety - Pyridazine - Benzenoid - 2-aminothiophene - Thiophene - Heteroaromatic compound - Vinylogous amide - Lactam - Ketone - Azacycle - Hydrocarbon derivative - Amine - Organic oxide - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - 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