Structure Information
Structure

Compound Identification

SMILES

COC1=CC=C(C=C1)N1[C@@H]([C@H]2COC(C)(C)O2)[C@@](F)(C1=O)C(C)(O)C1=CC=CC=C1

InChIKey

InChIKey=HYXTWCXIWDIBHE-VSOPNFGUSA-N

Formula

C23H26FNO5

Mass

415.461

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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

Phenylazetidines Methoxyanilines Phenoxy compounds Anisoles Methoxybenzenes Alkyl aryl ethers Ketals Tertiary carboxylic acid amides Tertiary alcohols 1,3-dioxolanes Fluorohydrins Oxacyclic compounds Azacyclic compounds Organofluorides Carbonyl compounds Organopnictogen compounds Aromatic alcohols Organonitrogen compounds Alkyl fluorides Hydrocarbon derivatives Organic oxides

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Monobactam - 1-phenylazetidine - Methoxyaniline - Phenoxy compound - Anisole - Phenol ether - Methoxybenzene - Alkyl aryl ether - Ketal - Monocyclic benzene moiety - Benzenoid - Tertiary carboxylic acid amide - Tertiary alcohol - Meta-dioxolane - Azetidine - Carboxamide group - Fluorohydrin - Halohydrin - Acetal - Azacycle - Oxacycle - Carboxylic acid derivative - Ether - Aromatic alcohol - Organopnictogen compound - Organohalogen compound - Organofluoride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic oxide - Organic oxygen compound - Alkyl halide - Alkyl fluoride - Organic nitrogen compound - Alcohol - Hydrocarbon derivative - 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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