Structure Information
Structure

Compound Identification

SMILES

[O-][N+](=O)C1=CC=C(COC(=O)C(N2C(CC2=O)S(=O)CC=C)C(=S)OC2=CC=C(F)C=C2)C=C1

InChIKey

InChIKey=HQEDVXLOPRWMRE-UHFFFAOYSA-N

Formula

C22H19FN2O7S2

Mass

506.52

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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 - Alpha-amino acid or derivatives - Benzyloxycarbonyl - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Halobenzene - Fluorobenzene - Aryl fluoride - Aryl halide - Benzenoid - Monocyclic benzene moiety - Tertiary carboxylic acid amide - Carboxylic acid ester - Azetidine - Sulfoxide - Thiocarboxylic acid ester - Allyl sulfur compound - Carboxamide group - Organic nitro compound - C-nitro compound - Carbothioic o-ester - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Allyl-type 1,3-dipolar organic compound - Sulfinyl compound - Thiocarboxylic acid or derivatives - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic nitrogen compound - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organic salt - Organic oxygen compound - Thiocarbonyl group - Organosulfur compound - Organohalogen compound - Carbonyl group - Organofluoride - 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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