Structure Information
Structure

Compound Identification

SMILES

CCOC(=O)C1=C(C=C(C=C1)[N+]([O-])=O)S(=O)(=O)NC(=O)NC1=NC(OC2=CC=CC=C2)=CC(Cl)=N1

InChIKey

InChIKey=MLTDWFCUUZXLBJ-UHFFFAOYSA-N

Formula

C20H16ClN5O8S

Mass

521.89

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organic nitrogen compounds

Class

Organonitrogen compounds

Subclass

Sulfonylureas

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidinyl-2-sulfonylureas

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidinyl-2-sulfonylurea - Nitrobenzoate - Diaryl ether - Benzenesulfonamide - Benzoate ester - Benzoic acid or derivatives - Benzenesulfonyl group - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Benzoyl - Phenol ether - Halopyrimidine - Aryl chloride - Aryl halide - Benzenoid - Monocyclic benzene moiety - Pyrimidine - Heteroaromatic compound - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Organic nitro compound - Carboxylic acid ester - C-nitro compound - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Ether - Allyl-type 1,3-dipolar organic compound - Azacycle - Organic oxoazanium - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic oxide - Organic zwitterion - Organic salt - Organochloride - Hydrocarbon derivative - Organic oxygen compound - Organohalogen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidinyl-2-sulfonylureas. These are aromatic heterocyclic compounds containing a pyrimidine ring which is substituted with a sulfonylurea at the ring 2-position.

External Descriptors

Not available

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