Structure Information
Structure

Compound Identification

SMILES

C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1[C@@H]([C@@H](C)C(=O)S[C@H]2CNC(=O)C2)N(C(=O)C(=O)OCC2=CC=C(C=C2)[N+]([O-])=O)C1=O

InChIKey

InChIKey=XFDDKPZIQNTGOS-YCPVIHDHSA-N

Formula

C27H37N3O9SSi

Mass

607.75

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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 or derivatives - Benzyloxycarbonyl - Nitrobenzene - Nitroaromatic compound - Monocyclic benzene moiety - Carboxylic acid imide, n-substituted - Pyrrolidone - 2-pyrrolidone - Benzenoid - Trialkylheterosilane - Dicarboximide - Carboxylic acid imide - Pyrrolidine - C-nitro compound - Carbothioic s-ester - Carboxylic acid ester - Azetidine - Secondary carboxylic acid amide - Thiocarboxylic acid ester - Carboxamide group - Silyl ether - Organic nitro compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic oxoazanium - Thiocarboxylic acid or derivatives - Azacycle - Organic 1,3-dipolar compound - Organoheterosilane - Sulfenyl compound - Organic metalloid salt - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxide - Organic metalloid moeity - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Organosilicon compound - Carbonyl group - Organic zwitterion - Organic oxygen compound - Organic salt - 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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