Compound Identification
SMILES
CN1C=NC2=C1N=C(NCC(C)(C)O)N=C2NCC1=C(O)C=CC(Cl)=C1
InChIKey
InChIKey=BAKOYFSFQNPGGV-UHFFFAOYSA-N
Formula
C17H21ClN6O2
Mass
376.85
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
P-chlorophenols Benzylamines Secondary alkylarylamines Chlorobenzenes Aminopyrimidines and derivatives 1-hydroxy-2-unsubstituted benzenoids N-substituted imidazoles Imidolactams Aryl chlorides Tertiary alcohols Heteroaromatic compounds Azacyclic compounds Organochlorides Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
6-alkylaminopurine - Benzylamine - 4-halophenol - 4-chlorophenol - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Halobenzene - Aminopyrimidine - Phenol - Secondary aliphatic/aromatic amine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Imidolactam - N-substituted imidazole - Benzenoid - Pyrimidine - Heteroaromatic compound - Imidazole - Azole - Tertiary alcohol - Azacycle - Secondary amine - Organochloride - Organohalogen compound - Amine - Alcohol - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic nitrogen compound - 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