Compound Identification
SMILES
CC1=CC(OS(=O)(=O)C(F)(F)F)=C(C(=O)CCC2=CC=CO2)C(=O)O1
InChIKey
InChIKey=NQYNOAOGHDMARE-UHFFFAOYSA-N
Formula
C14H11F3O7S
Mass
380.29
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Organic acids and derivatives
-
Class
Organic sulfonic acids and derivatives
-
Subclass
Organosulfonic acids and derivatives
-
Level 5
Alkanesulfonic acids and derivatives
-
Level 6
Alkanesulfonic acids
- Level 7 Trifluoromethanesulfonates
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Level 6
Alkanesulfonic acids
-
Level 5
Alkanesulfonic acids and derivatives
-
Subclass
Organosulfonic acids and derivatives
-
Class
Organic sulfonic acids and derivatives
-
Superclass
Organic acids and derivatives
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
Organic sulfonic acids and derivatives
Subclass
Organosulfonic acids and derivatives
Intermediate Tree Nodes
Alkanesulfonic acids and derivatives - Alkanesulfonic acids
Direct Parent
Trifluoromethanesulfonates
Alternative Parents
Aryl alkyl ketones Pyranones and derivatives Sulfonic acid esters Organosulfonic acid esters Sulfonyls Methanesulfonates Heteroaromatic compounds Furans Trihalomethanes Lactones Oxacyclic compounds Organofluorides Organic oxides Hydrocarbon derivatives Alkyl fluorides
Molecular Framework
Aromatic heteromonocyclic compounds
Substituents
Trifluoromethanesulfonate - Aryl ketone - Aryl alkyl ketone - Pyranone - Pyran - Sulfonic acid ester - Organosulfonic acid ester - Furan - Methanesulfonate - Sulfonyl - Heteroaromatic compound - Trihalomethane - Lactone - Ketone - Organoheterocyclic compound - Oxacycle - Halomethane - Organic oxide - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Organofluoride - Organohalogen compound - Alkyl halide - Hydrocarbon derivative - Alkyl fluoride - Aromatic heteromonocyclic compound
Description
This compound belongs to the class of organic compounds known as trifluoromethanesulfonates. These are alkanesulfonic acids, that contain a sulfonate group that is substituted with a trifluoromethyl group.
External Descriptors
Not available