Structure Information
Structure

Compound Identification

SMILES

CC(=O)S[C@@H]1[C@@H](OC(=O)COC2=CC=CC=C2)C(=O)N1C(Cl)C(=O)OCC1=CC=C(C=C1)[N+]([O-])=O

InChIKey

InChIKey=CCSJFQGBZCUTEB-OWJBEEKMSA-N

Formula

C22H19ClN2O9S

Mass

522.91

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Organoheterocyclic compounds

Class

Lactams

Subclass

Beta lactams

Intermediate Tree Nodes

Not available

Direct Parent

Monobactams

Alternative Parents

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Monobactam - Alpha-amino acid ester - Phenoxyacetate - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenol ether - Alkyl aryl ether - Dicarboxylic acid or derivatives - Monocyclic benzene moiety - Benzenoid - Alpha-halocarboxylic acid derivative - Alpha-halocarboxylic acid or derivatives - Tertiary carboxylic acid amide - Carbothioic s-ester - Thiocarboxylic acid ester - C-nitro compound - Organic nitro compound - Azetidine - Carboxylic acid ester - Carboxamide group - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Sulfenyl compound - Ether - Hemithioaminal - Thiocarboxylic acid or derivatives - Organic oxoazanium - Organic zwitterion - Organic oxide - Organic oxygen compound - Carbonyl group - Alkyl halide - Hydrocarbon derivative - Organic nitrogen compound - Organic salt - Organosulfur compound - Organohalogen compound - Alkyl chloride - Organochloride - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as monobactams. These are compounds comprising beta-lactam ring is alone and not fused to another ring.

External Descriptors

Not available

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