ChemFOnt: Showing chemical card for [4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid (CFc000125924)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:52:56 UTC

Chemfont ID

CFc000125924

Molecule Identification

Common Name

[4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid

Definition

[4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid belongs to the class of organic compounds known as 4-hydroxycoumarins. These are coumarins that contain one or more hydroxyl groups attached to C4-position the coumarin skeleton. Based on a literature review very few articles have been published on [4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid.

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
[4-(4-Hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonate	Generator
[4-(4-Hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulphonate	Generator
[4-(4-Hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulphonic acid	Generator

Chemical Formula

C₁₉H₁₅NO₁₀S

Average Molecular Weight

449.39

Monoisotopic Molecular Weight

449.041666861

IUPAC Name

[4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid

Traditional Name

4-(4-hydroxy-2-oxochromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxysulfonic acid

CAS Registry Number

Not Available

SMILES

OC1=C(C(CC(=O)COS(O)(=O)=O)C2=CC=C(C=C2)N(=O)=O)C(=O)OC2=CC=CC=C12

InChI Identifier

InChI=1S/C19H15NO10S/c21-13(10-29-31(26,27)28)9-15(11-5-7-12(8-6-11)20(24)25)17-18(22)14-3-1-2-4-16(14)30-19(17)23/h1-8,15,22H,9-10H2,(H,26,27,28)

InChI Key

YKSNLGDXCXFGSM-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 4-hydroxycoumarins. These are coumarins that contain one or more hydroxyl groups attached to C4-position the coumarin skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Coumarins and derivatives

Sub Class

Hydroxycoumarins

Direct Parent

4-hydroxycoumarins

Alternative Parents

Substituents

4-hydroxycoumarin
Benzopyran
1-benzopyran
Nitrobenzene
Nitroaromatic compound
Pyranone
Monocyclic benzene moiety
Pyran
Sulfuric acid monoester
Sulfate-ester
Alkyl sulfate
Benzenoid
Sulfuric acid ester
Heteroaromatic compound
Organic sulfuric acid or derivatives
Vinylogous acid
Ketone
Lactone
C-nitro compound
Organic nitro compound
Organoheterocyclic compound
Oxacycle
Organic oxoazanium
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Allyl-type 1,3-dipolar organic compound
Hydrocarbon derivative
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organic oxide
Organopnictogen compound
Carbonyl group
Organic oxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Exogenous (HMDB: HMDB0145515)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.026 g/L	ALOGPS
logP	0.72	ALOGPS
logP	1.92	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	-2.2	ChemAxon
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	173.02 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	105.88 m³·mol⁻¹	ChemAxon
Polarizability	40.68 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	Yes	ChemAxon

External Links

HMDB ID

HMDB0145515

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 [4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid (CFc000125924)

MOL for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

3D MOL for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

3D SDF for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

3D-SDF for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

PDB for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

3D PDB for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

SMILES for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

INCHI for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

Structure for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)

3D Structure for CFc000125924 ([4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-4-(4-nitrophenyl)-2-oxobutoxy]sulfonic acid)