Compound Identification
SMILES
CN(C)C1=CC=C(C=NC2=CC=C(C=C2)N2C(CC3=CC=CC=C3NC3=C(Cl)C=CC=C3Cl)=NC3=C(C=C(Br)C=C3)C2=O)C=C1
InChIKey
InChIKey=GHCDMYUSLBJSEP-UHFFFAOYSA-N
Formula
C36H28BrCl2N5O
Mass
697.46
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Diazanaphthalenes
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Subclass
Benzodiazines
- Level 5 Quinazolines
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Subclass
Benzodiazines
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Class
Diazanaphthalenes
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazanaphthalenes
Subclass
Benzodiazines
Intermediate Tree Nodes
Not available
Direct Parent
Quinazolines
Alternative Parents
Aniline and substituted anilines Dialkylarylamines Dichlorobenzenes Pyrimidones Aryl bromides Aryl chlorides Primary aromatic amines Heteroaromatic compounds Lactams Shiff bases Propargyl-type 1,3-dipolar organic compounds Secondary amines Azacyclic compounds Organobromides Organic oxides Hydrocarbon derivatives Organochlorides Organooxygen compounds
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Quinazoline - 1,3-dichlorobenzene - Tertiary aliphatic/aromatic amine - Aniline or substituted anilines - Dialkylarylamine - Chlorobenzene - Halobenzene - Pyrimidone - Aryl bromide - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Primary aromatic amine - Pyrimidine - Benzenoid - Heteroaromatic compound - Tertiary amine - Shiff base - Lactam - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Aldimine - Azacycle - Secondary amine - Hydrocarbon derivative - Organohalogen compound - Imine - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organobromide - Organochloride - Organonitrogen compound - Organooxygen compound - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as quinazolines. These are compounds containing a quinazoline moiety, which is made up of two fused six-member aromatic rings, a benzene ring and a pyrimidine ring.
External Descriptors
Not available