Structure Information
Structure

Compound Identification

SMILES

CO[C@@H]1\C=C\C=C(C)\CC2=CC(N(C)C(=O)C[C@H](O[Si](C)(C)C(C)(C)C)\C(C)=C\[C@H](C)[C@@H]3C[C@@]1(O)NC(=O)O3)=C(Cl)C(OC)=C2

InChIKey

InChIKey=YQBKAPPJTRULKH-HBEXAGBXSA-N

Formula

C34H51ClN2O7Si

Mass

663.32

Export to:

JSON SDF CSV

Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Phenylpropanoids and polyketides

Class

Macrolactams

Subclass

Not available

Intermediate Tree Nodes

Not available

Direct Parent

Macrolactams

Alternative Parents

Molecular Framework

Aromatic heteropolycyclic compounds

Substituents

Macrolactam - Anisole - Phenol ether - Alkyl aryl ether - 1,3-oxazinane - Aryl chloride - Aryl halide - Oxazinane - Benzenoid - Trialkylheterosilane - Carbamic acid ester - Tertiary carboxylic acid amide - Carboxamide group - Lactam - Silyl ether - Alkanolamine - Organoheterosilane - Oxacycle - Carboxylic acid derivative - Dialkyl ether - Ether - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Carbonyl group - Organohalogen compound - Organic metalloid moeity - Organochloride - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organosilicon compound - Aromatic heteropolycyclic compound

Description

This compound belongs to the class of organic compounds known as macrolactams. These are cyclic amides of amino carboxylic acids, having a 1-azacycloalkan-2-one structure, or analogues having unsaturation or heteroatoms replacing one or more carbon atoms of the ring. They are nitrogen analogues (the a nitrogen atom replacing the o atom of the cyclic carboxylic acid group ) of the naturally occurring macrolides.

External Descriptors

Not available

Previous Back Next