Structure Information
Structure

Compound Identification

SMILES

CC[C@H]1[C@H](Cl)N(\C(C(=O)OCC2=CC=C(C=C2)[N+]([O-])=O)=C(\OC2=CC=CC=C2)SC(=O)C(C)(C)C)C1=O

InChIKey

InChIKey=CSUOJUQDKPCYKH-QBDOQLORSA-N

Formula

C26H27ClN2O7S

Mass

547.02

Export to:

JSON SDF CSV

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 or derivatives - Benzyloxycarbonyl - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Monocyclic benzene moiety - Benzenoid - Monothioacetal - Tertiary carboxylic acid amide - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous ester - Organic nitro compound - Azetidine - Carbothioic s-ester - Thiocarboxylic acid ester - Carboxamide group - Carboxylic acid ester - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Sulfenyl compound - Thiocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxoazanium - Azacycle - Organic nitrogen compound - Organic salt - Organohalogen compound - Alkyl chloride - Organochloride - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Carbonyl group - Organic oxide - Organic oxygen compound - Alkyl halide - Organic cation - 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

Previous Back Next