Structure Information
Structure

Compound Identification

SMILES

OCC1OC(CC1O)N1C=C(N=CC2=C(Cl)C=C(Cl)C=C2)C(=O)NC1=O

InChIKey

InChIKey=MVGFKQDCIPTEGV-UHFFFAOYSA-N

Formula

C16H15Cl2N3O5

Mass

400.21

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Nucleosides, nucleotides, and analogues

Class

Pyrimidine nucleosides

Subclass

Pyrimidine 2'-deoxyribonucleosides

Intermediate Tree Nodes

Not available

Direct Parent

Pyrimidine 2'-deoxyribonucleosides

Alternative Parents

Dichlorobenzenes Pyrimidones Aryl chlorides Hydropyrimidines Vinylogous amides Oxolanes Heteroaromatic compounds Ureas Shiff bases Secondary alcohols Lactams Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Oxacyclic compounds Primary alcohols Hydrocarbon derivatives Organochlorides Organic oxides

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside - 1,3-dichlorobenzene - Chlorobenzene - Halobenzene - Pyrimidone - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Hydropyrimidine - Pyrimidine - Benzenoid - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Shiff base - Secondary alcohol - Lactam - Oxacycle - Aldimine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Hydrocarbon derivative - Organohalogen compound - Imine - Alcohol - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Primary alcohol - Aromatic heteromonocyclic compound

Description

This compound belongs to the class of organic compounds known as pyrimidine 2'-deoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at position 2.

External Descriptors

Not available

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