Compound Identification
SMILES
CCN(C([O-])=O)C1=NC(Cl)=C(C(N)=C1)[N+]([O-])=O
InChIKey
InChIKey=PUGWPZHJEREUDX-UHFFFAOYSA-M
Formula
C8H8ClN4O4
Mass
259.63
Taxonomic Classification
Taxonomy Tree
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Kingdom
Organic compounds
-
Superclass
Organic 1,3-dipolar compounds
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Class
Allyl-type 1,3-dipolar organic compounds
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Subclass
Organic nitro compounds
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Level 5
C-nitro compounds
- Level 6 Nitroaromatic compounds
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Level 5
C-nitro compounds
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Subclass
Organic nitro compounds
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Class
Allyl-type 1,3-dipolar organic compounds
-
Superclass
Organic 1,3-dipolar compounds
Kingdom
Organic compounds
Superclass
Organic 1,3-dipolar compounds
Class
Allyl-type 1,3-dipolar organic compounds
Subclass
Organic nitro compounds
Intermediate Tree Nodes
C-nitro compounds
Direct Parent
Nitroaromatic compounds
Alternative Parents
2-halopyridines Aminopyridines and derivatives Aryl chlorides Imidolactams Heteroaromatic compounds Tertiary amines Carbamic acids Organic oxoazanium compounds Azacyclic compounds Hydrocarbon derivatives Organic salts Carbonyl compounds Primary amines Organochlorides Organic oxides Organic cations
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Nitroaromatic compound - Aminopyridine - 2-halopyridine - Aryl chloride - Aryl halide - Pyridine - Imidolactam - Heteroaromatic compound - Carbamic acid - Carbamic acid derivative - Tertiary amine - Organoheterocyclic compound - Azacycle - Organic oxoazanium - Amine - Organic salt - Primary amine - Organooxygen compound - Organonitrogen compound - Organochloride - Hydrocarbon derivative - Organohalogen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Organic oxygen compound - Organic cation - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as nitroaromatic compounds. These are c-nitro compounds where the nitro group is C-substituted with an aromatic group.
External Descriptors
Not available