Compound Identification
SMILES
CSC(=N\C=C\C1=CN(COCC2=CC=CC=C2)C(SC)=N1)C1=CC(Br)=C(Br)N1COCC1=CC=CC=C1
InChIKey
InChIKey=CZVBDDBAQZYTSF-SCHXYESCSA-N
Formula
C28H28Br2N4O2S2
Mass
676.49
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organoheterocyclic compounds
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Class
Azoles
-
Subclass
Imidazoles
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Level 5
Substituted imidazoles
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Level 6
Trisubstituted imidazoles
- Level 7 1,2,4-trisubstituted imidazoles
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Level 6
Trisubstituted imidazoles
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Level 5
Substituted imidazoles
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Subclass
Imidazoles
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Class
Azoles
-
Superclass
Organoheterocyclic compounds
Kingdom
Organic compounds
Superclass
Organoheterocyclic compounds
Class
Azoles
Subclass
Imidazoles
Intermediate Tree Nodes
Substituted imidazoles - Trisubstituted imidazoles
Direct Parent
1,2,4-trisubstituted imidazoles
Alternative Parents
Alkylarylthioethers Substituted pyrroles N-substituted imidazoles Benzene and substituted derivatives Aryl bromides Heteroaromatic compounds Imidothioesters Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Imidothioic acids and derivatives Azacyclic compounds Organooxygen compounds Organonitrogen compounds Organobromides Hydrocarbon derivatives
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
1,2,4-trisubstituted-imidazole - Aryl thioether - Alkylarylthioether - Aryl bromide - Aryl halide - Monocyclic benzene moiety - N-substituted imidazole - Benzenoid - Substituted pyrrole - Heteroaromatic compound - Pyrrole - Imidothioester - Azacycle - Organic 1,3-dipolar compound - Imidothioic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Sulfenyl compound - Thioether - Organohalogen compound - Hydrocarbon derivative - Organic oxygen compound - Organobromide - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as 1,2,4-trisubstituted imidazoles. These are imidazoles in which the imidazole ring is substituted at positions 1, 2, and 3.
External Descriptors
Not available