ChemFOnt: Showing chemical card for {2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid (CFc000126604)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:54:02 UTC

Chemfont ID

CFc000126604

Molecule Identification

Common Name

{2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid

Definition

{2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic 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 {2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
{2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonate	Generator
{2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulphonate	Generator
{2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulphonic acid	Generator

Chemical Formula

C₁₄H₁₂O₈S

Average Molecular Weight

340.3

Monoisotopic Molecular Weight

340.02528852

IUPAC Name

{2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid

Traditional Name

{2,2-dimethyl-4,8-dioxo-3H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

CC1(C)OC2=C(C=C3C=CC(=O)OC3=C2)C(=O)C1OS(O)(=O)=O

InChI Identifier

InChI=1S/C14H12O8S/c1-14(2)13(22-23(17,18)19)12(16)8-5-7-3-4-11(15)20-9(7)6-10(8)21-14/h3-6,13H,1-2H3,(H,17,18,19)

InChI Key

NETXTFIPYUSBIW-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
2,2-dimethyl-1-benzopyran
Chromone
Chromane
Benzopyran
1-benzopyran
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Sulfuric acid ester
Organic sulfuric acid or derivatives
Heteroaromatic compound
Lactone
Ketone
Organoheterocyclic compound
Ether
Oxacycle
Organooxygen compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Exogenous (HMDB: HMDB0146195)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.28 g/L	ALOGPS
logP	0.28	ALOGPS
logP	1.16	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	-2.1	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	116.2 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	76.94 m³·mol⁻¹	ChemAxon
Polarizability	31.07 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

HMDB0146195

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 {2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid (CFc000126604)

MOL for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

3D MOL for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

3D SDF for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

3D-SDF for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

PDB for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

3D PDB for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

SMILES for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

INCHI for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

Structure for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)

3D Structure for CFc000126604 ({2,2-dimethyl-4,8-dioxo-2H,3H,4H,8H-pyrano[3,2-g]chromen-3-yl}oxidanesulfonic acid)