Compound Identification
SMILES
C1CC=C(C=C1)[C@H]1CC=C(C=C1)N([C@@H]1CC=C(C=C1)[C@@H]1CC=CC=C1)C1=CC(=CCC1)C1CC=C(C=C1)[C@@H]1NC(=CC(=N1)C1=CC=C(CC1)C1=CC=CCC1)[C@@H]1CC=C(C=C1)[C@@H]1CC=CC=C1
InChIKey
InChIKey=SZUUHSRSPSNERP-AFOUQNNYSA-N
Formula
C64H67N3
Mass
878.261
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Diazines
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Subclass
Pyrimidines and pyrimidine derivatives
- Level 5 Hydropyrimidines
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Subclass
Pyrimidines and pyrimidine derivatives
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Class
Diazines
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Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Diazines
Subclass
Pyrimidines and pyrimidine derivatives
Intermediate Tree Nodes
Not available
Direct Parent
Hydropyrimidines
Alternative Parents
Trialkylamines Ketimines Propargyl-type 1,3-dipolar organic compounds Enamines Azacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
1,2-dihydropyrimidine - Hydropyrimidine - Tertiary aliphatic amine - Tertiary amine - Ketimine - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Enamine - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Imine - Amine - Aliphatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as hydropyrimidines. These are compounds containing a hydrogenated pyrimidine ring (i.e. containing less than the maximum number of double bonds.).
External Descriptors
Not available