Compound Identification
SMILES
CC1(C)OCCC(=C1)C1=NC=C2OC3=C(C=C(C=C3)C3=CN=C(F)C=C3)[C@@]3(COC(N)=N3)C2=C1
InChIKey
InChIKey=PKQIVXKNXZECPO-SANMLTNESA-N
Formula
C26H23FN4O3
Mass
458.493
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Benzopyrans
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Subclass
1-benzopyrans
- Level 5 Chromenopyridines
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Subclass
1-benzopyrans
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Class
Benzopyrans
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Benzopyrans
Subclass
1-benzopyrans
Intermediate Tree Nodes
Not available
Direct Parent
Chromenopyridines
Alternative Parents
Diarylethers Pyranopyridines 2-halopyridines Pyrans Aryl fluorides Benzenoids Oxazolines Heteroaromatic compounds Isoureas Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Azacyclic compounds Carboximidamides Dialkyl ethers Amines Organopnictogen compounds Organofluorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Chromenopyridine - Diaryl ether - Pyranopyridine - 2-halopyridine - Aryl fluoride - Aryl halide - Pyran - Benzenoid - Pyridine - Heteroaromatic compound - Oxazoline - Isourea - Dialkyl ether - Ether - Oxacycle - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organohalogen compound - Organic nitrogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organopnictogen compound - Amine - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as chromenopyridines. These are aromatic heterocyclic compounds structurally characterized by a pyridine ring fused to a chromene moiety.
External Descriptors
Not available