ChemFOnt: Showing chemical card for 6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000146522)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:26:10 UTC

Chemfont ID

CFc000146522

Molecule Identification

Common Name

6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Definition

6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. Based on a literature review very few articles have been published on 6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
6-(2-Formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylate	Generator

Chemical Formula

C₁₃H₁₄O₈

Average Molecular Weight

298.247

Monoisotopic Molecular Weight

298.068867411

IUPAC Name

6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

Traditional Name

6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

OC1C(OC2=CC=CC=C2C=O)OC(C(O)C1O)C(O)=O

InChI Identifier

InChI=1S/C13H14O8/c14-5-6-3-1-2-4-7(6)20-13-10(17)8(15)9(16)11(21-13)12(18)19/h1-5,8-11,13,15-17H,(H,18,19)

InChI Key

ZFLOPNPEOJNESA-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
1-o-glucuronide
O-glucuronide
Glucuronic acid or derivatives
Hexose monosaccharide
O-glycosyl compound
Phenoxy compound
Benzaldehyde
Benzoyl
Phenol ether
Beta-hydroxy acid
Aryl-aldehyde
Pyran
Monocyclic benzene moiety
Hydroxy acid
Monosaccharide
Benzenoid
Oxane
Secondary alcohol
Organoheterocyclic compound
Oxacycle
Carboxylic acid
Carboxylic acid derivative
Acetal
Monocarboxylic acid or derivatives
Polyol
Aldehyde
Carbonyl group
Hydrocarbon derivative
Organic oxide
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	17.3 g/L	ALOGPS
logP	-0.79	ALOGPS
logP	-0.57	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	3.11	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	133.52 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	66.63 m³·mol⁻¹	ChemAxon
Polarizability	27.24 Å³	ChemAxon
Number of Rings	2	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

HMDB0166114

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 6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid (CFc000146522)

MOL for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D MOL for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D SDF for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D-SDF for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

PDB for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D PDB for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

SMILES for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

INCHI for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

Structure for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)

3D Structure for CFc000146522 (6-(2-formylphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic acid)