Compound Identification
SMILES
ClC1=NC2=C(N=CN2CCCC2=CC=CC=C2)C(NCC2=CC=C(Br)C=C2)=N1
InChIKey
InChIKey=JORLFOQNVQYKEP-UHFFFAOYSA-N
Formula
C21H19BrClN5
Mass
456.77
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
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Superclass
Organoheterocyclic compounds
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Class
Imidazopyrimidines
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Subclass
Purines and purine derivatives
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Level 5
6-aminopurines
- Level 6 6-alkylaminopurines
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Level 5
6-aminopurines
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Subclass
Purines and purine derivatives
-
Class
Imidazopyrimidines
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Imidazopyrimidines
Subclass
Purines and purine derivatives
Intermediate Tree Nodes
6-aminopurines
Direct Parent
6-alkylaminopurines
Alternative Parents
Benzylamines Bromobenzenes Aminopyrimidines and derivatives 2-halopyrimidines N-substituted imidazoles Imidolactams Aryl chlorides Aryl bromides Heteroaromatic compounds Azacyclic compounds Organochlorides Organobromides Hydrocarbon derivatives Amines
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
6-alkylaminopurine - Benzylamine - Aminopyrimidine - 2-halopyrimidine - Bromobenzene - Halobenzene - Halopyrimidine - Aryl bromide - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Imidolactam - N-substituted imidazole - Pyrimidine - Benzenoid - Heteroaromatic compound - Imidazole - Azole - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organohalogen compound - Organobromide - Organochloride - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as 6-alkylaminopurines. These are compounds that contain an alkylamine group attached at the 6-position of a purine. Purine is a bicyclic aromatic compound made up of a pyrimidine ring fused to an imidazole ring.
External Descriptors
Not available