ChemFOnt: Showing chemical card for [(9-hydroxy-6-oxononyl)oxy]sulfonic acid (CFc000159595)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:47:37 UTC

Chemfont ID

CFc000159595

Molecule Identification

Common Name

[(9-hydroxy-6-oxononyl)oxy]sulfonic acid

Definition

[(9-hydroxy-6-oxononyl)oxy]sulfonic acid belongs to the class of organic compounds known as sulfuric acid monoesters. These are organic compounds containing the sulfuric acid monoester functional group, with the generic structure ROS(O)(=O)=O, (R=organyl group). Based on a literature review a significant number of articles have been published on [(9-hydroxy-6-oxononyl)oxy]sulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
[(9-Hydroxy-6-oxononyl)oxy]sulfonate	Generator
[(9-Hydroxy-6-oxononyl)oxy]sulphonate	Generator
[(9-Hydroxy-6-oxononyl)oxy]sulphonic acid	Generator

Chemical Formula

C₉H₁₈O₆S

Average Molecular Weight

254.3

Monoisotopic Molecular Weight

254.082409474

IUPAC Name

[(9-hydroxy-6-oxononyl)oxy]sulfonic acid

Traditional Name

(9-hydroxy-6-oxononyl)oxysulfonic acid

CAS Registry Number

Not Available

SMILES

OCCCC(=O)CCCCCOS(O)(=O)=O

InChI Identifier

InChI=1S/C9H18O6S/c10-7-4-6-9(11)5-2-1-3-8-15-16(12,13)14/h10H,1-8H2,(H,12,13,14)

InChI Key

GJJRQDRJXLNQBM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as sulfuric acid monoesters. These are organic compounds containing the sulfuric acid monoester functional group, with the generic structure ROS(O)(=O)=O, (R=organyl group).

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Organic sulfuric acids and derivatives

Sub Class

Sulfuric acid esters

Direct Parent

Sulfuric acid monoesters

Alternative Parents

Substituents

Alkyl sulfate
Sulfate-ester
Sulfuric acid monoester
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	2.7 g/L	ALOGPS
logP	-1.2	ALOGPS
logP	-1.1	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	-1.7	ChemAxon
pKa (Strongest Basic)	-2.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	100.9 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	57.7 m³·mol⁻¹	ChemAxon
Polarizability	25.9 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0179187

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for [(9-hydroxy-6-oxononyl)oxy]sulfonic acid (CFc000159595)

MOL for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

3D MOL for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

3D SDF for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

3D-SDF for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

PDB for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

3D PDB for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

SMILES for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

INCHI for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

Structure for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)

3D Structure for CFc000159595 ([(9-hydroxy-6-oxononyl)oxy]sulfonic acid)