Compound Identification
SMILES
Cl.CN(C)C1=CC2=C(C=C1C)N(C)C1(OC3=C(CO)C=C(C=C3C=C1)[N+]([O-])=O)[Se]2
InChIKey
InChIKey=KRAZSZWVFOEJCG-UHFFFAOYSA-N
Formula
C20H22ClN3O4Se
Mass
482.83
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
-
Class
Benzopyrans
- Subclass 1-benzopyrans
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Class
Benzopyrans
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Benzopyrans
Subclass
1-benzopyrans
Intermediate Tree Nodes
Not available
Direct Parent
1-benzopyrans
Alternative Parents
Diaminotoluenes Nitroaromatic compounds Dialkylarylamines Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organic oxoazanium compounds Azacyclic compounds Primary alcohols Organoselenium compounds Organic zwitterions Organic oxides Hydrochlorides Hydrocarbon derivatives Aromatic alcohols
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
1-benzopyran - Diaminotoluene - Nitroaromatic compound - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Benzenoid - C-nitro compound - Tertiary amine - Organic nitro compound - Organic oxoazanium - Oxacycle - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Azacycle - Amine - Organic zwitterion - Hydrocarbon derivative - Aromatic alcohol - Organic oxide - Organic oxygen compound - Primary alcohol - Organoselenium compound - Organooxygen compound - Organic nitrogen compound - Alcohol - Organic salt - Organonitrogen compound - Hydrochloride - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 1-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 1-position.
External Descriptors
Not available