Showing chemical card for (2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid (CFc000147133)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 23:27:10 UTC

Chemfont ID

CFc000147133

Molecule Identification

Common Name

(2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid

Definition

(2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid belongs to the class of organic compounds known as phenylsulfates. Phenylsulfates are compounds containing a sulfuric acid group conjugated to a phenyl group. Based on a literature review very few articles have been published on (2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid.

Structure

MOL SDF PDB SMILES InChI

MOL for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

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3D MOL for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

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3D SDF for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

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3D-SDF for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

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PDB for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

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3D PDB for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

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SMILES for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

CC1=CC(=C(OS(O)(=O)=O)C(=C1)C(C)(C)C)C(C)(C)C

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INCHI for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

InChI=1S/C15H24O4S/c1-10-8-11(14(2,3)4)13(19-20(16,17)18)12(9-10)15(5,6)7/h8-9H,1-7H3,(H,16,17,18)

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Structure for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

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3D Structure for CFc000147133 ((2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid)

Synonyms

Value	Source
(2,6-Di-tert-butyl-4-methylphenyl)oxidanesulfonate	Generator
(2,6-Di-tert-butyl-4-methylphenyl)oxidanesulphonate	Generator
(2,6-Di-tert-butyl-4-methylphenyl)oxidanesulphonic acid	Generator

Chemical Formula

C₁₅H₂₄O₄S

Average Molecular Weight

300.41

Monoisotopic Molecular Weight

300.139530427

IUPAC Name

(2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid

Traditional Name

(2,6-di-tert-butyl-4-methylphenyl)oxidanesulfonic acid

CAS Registry Number

Not Available

SMILES

CC1=CC(=C(OS(O)(=O)=O)C(=C1)C(C)(C)C)C(C)(C)C

InChI Identifier

InChI=1S/C15H24O4S/c1-10-8-11(14(2,3)4)13(19-20(16,17)18)12(9-10)15(5,6)7/h8-9H,1-7H3,(H,16,17,18)

InChI Key

LSJVEKHJTJZYMY-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenylsulfates. Phenylsulfates are compounds containing a sulfuric acid group conjugated to a phenyl group.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Organic sulfuric acids and derivatives

Sub Class

Arylsulfates

Direct Parent

Phenylsulfates

Alternative Parents

Phenylpropanes
Phenoxy compounds
Toluenes
Sulfuric acid monoesters
Organooxygen compounds
Organic oxides
Hydrocarbon derivatives

Substituents

Phenylsulfate
Phenylpropane
Phenoxy compound
Toluene
Benzenoid
Sulfuric acid ester
Sulfate-ester
Sulfuric acid monoester
Monocyclic benzene moiety
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Not Available

Not Available

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.014 g/L	ALOGPS
logP	1.87	ALOGPS
logP	4.8	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	-1.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	63.6 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	80.4 m³·mol⁻¹	ChemAxon
Polarizability	32.18 Å³	ChemAxon
Number of Rings	1	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

HMDB0166725

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

159442864

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available