Structure Information
Structure

Compound Identification

SMILES

CC1CC(C)(C)NC(CCOP(=O)(OC[C@H]2O[C@H](C[C@@H]2O[Si](C)(C)C(C)(C)C)N2C=C(F)C(=O)NC2=O)N(C)CCCl)O1

InChIKey

InChIKey=KHRKJZWVBGAFMR-KOTPVDECSA-N

Formula

C27H49ClFN4O8PSi

Mass

671.22

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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

Molecular Framework

Aromatic heteromonocyclic compounds

Substituents

Pyrimidine 2'-deoxyribonucleoside - Phosphoric diester monoamide - Pyrimidone - Halopyrimidine - 1,3-oxazinane - Pyrimidine - Aryl fluoride - Organic phosphoric acid amide - Aryl halide - Hydropyrimidine - Organic phosphoric acid derivative - Oxazinane - Phosphoric acid ester - Trialkylheterosilane - Heteroaromatic compound - Oxolane - Vinylogous amide - Hemiaminal - Lactam - Silyl ether - Urea - Organoheterocyclic compound - Organic metalloid salt - Azacycle - Secondary amine - Organoheterosilane - Oxacycle - Organooxygen compound - Organochloride - Organofluoride - Organic metalloid moeity - Organohalogen compound - Alkyl chloride - Hydrocarbon derivative - Organic nitrogen compound - Organic oxide - Organonitrogen compound - Organic oxygen compound - Alkyl halide - Organosilicon compound - Amine - 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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