ChemFOnt: Showing chemical card for ({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid (CFc000127642)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:55:37 UTC

Chemfont ID

CFc000127642

Molecule Identification

Common Name

({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid

Definition

({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid belongs to the class of organic compounds known as linear pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety. Based on a literature review very few articles have been published on ({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonate	Generator
({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulphonate	Generator
({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulphonic acid	Generator

Chemical Formula

C₁₅H₁₄O₈S

Average Molecular Weight

354.33

Monoisotopic Molecular Weight

354.040938585

IUPAC Name

({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid

Traditional Name

{5-methoxy-2-methyl-8-oxopyrano[3,2-g]chromen-2-yl}methoxysulfonic acid

CAS Registry Number

Not Available

SMILES

COC1=C2C=CC(=O)OC2=CC2=C1C=CC(C)(COS(O)(=O)=O)O2

InChI Identifier

InChI=1S/C15H14O8S/c1-15(8-21-24(17,18)19)6-5-10-12(23-15)7-11-9(14(10)20-2)3-4-13(16)22-11/h3-7H,8H2,1-2H3,(H,17,18,19)

InChI Key

GMMFWEWJPZJKIB-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as linear pyranocoumarins. These are organic compounds containing a pyran (or a hydrogenated derivative) linearly fused to a coumarin moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Pyranocoumarins

Direct Parent

Linear pyranocoumarins

Alternative Parents

Substituents

Linear pyranocoumarin
Pyranochromene
Benzopyran
1-benzopyran
Anisole
Alkyl aryl ether
Pyranone
Pyran
Sulfuric acid monoester
Benzenoid
Sulfuric acid ester
Alkyl sulfate
Sulfate-ester
Organic sulfuric acid or derivatives
Heteroaromatic compound
Lactone
Ether
Oxacycle
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Exogenous (HMDB: HMDB0147233)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.096 g/L	ALOGPS
logP	0.05	ALOGPS
logP	1.53	ChemAxon
logS	-3.6	ALOGPS
pKa (Strongest Acidic)	-2.2	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	108.36 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	83.94 m³·mol⁻¹	ChemAxon
Polarizability	33.39 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0147233

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 ({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid (CFc000127642)

MOL for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

3D MOL for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

3D SDF for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

3D-SDF for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

PDB for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

3D PDB for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

SMILES for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

INCHI for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

Structure for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)

3D Structure for CFc000127642 (({5-methoxy-2-methyl-8-oxo-2H,8H-pyrano[3,2-g]chromen-2-yl}methoxy)sulfonic acid)