ChemFOnt: Showing chemical card for 3-(2-methoxyphenyl)prop-2-enoic acid (CFc000127026)

Record Information

Version

1.0

Creation Date

2022-08-28 10:25:12 UTC

Update Date

2022-09-13 21:54:40 UTC

Chemfont ID

CFc000127026

Molecule Identification

Common Name

3-(2-methoxyphenyl)prop-2-enoic acid

Definition

(Z)-3-(2-Methoxyphenyl)acrylic acid belongs to the class of organic compounds known as coumaric acids. These are aromatic compounds containing a cinnamic acid moiety hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring (Z)-3-(2-Methoxyphenyl)acrylic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI

Synonyms

Value	Source
(Z)-3-(2-Methoxyphenyl)acrylate	Generator
3-(2-Methoxyphenyl)prop-2-enoate	Generator

Chemical Formula

C₁₀H₁₀O₃

Average Molecular Weight

178.187

Monoisotopic Molecular Weight

178.062994182

IUPAC Name

3-(2-methoxyphenyl)prop-2-enoic acid

Traditional Name

3-(2-methoxyphenyl)prop-2-enoic acid

CAS Registry Number

Not Available

SMILES

COC1=CC=CC=C1C=CC(O)=O

InChI Identifier

InChI=1S/C10H10O3/c1-13-9-5-3-2-4-8(9)6-7-10(11)12/h2-7H,1H3,(H,11,12)

InChI Key

FEGVSPGUHMGGBO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumaric acids. These are aromatic compounds containing a cinnamic acid moiety hydroxylated at the C2 (ortho-), C3 (meta-), or C4 (para-) carbon atom of the benzene ring.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Hydroxycinnamic acids and derivatives

Direct Parent

Coumaric acids

Alternative Parents

Substituents

Cinnamic acid
Coumaric acid
Phenoxy compound
Anisole
Methoxybenzene
Styrene
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Ether
Organic oxygen compound
Carbonyl group
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Exogenous (HMDB: HMDB0146617)

Process

Not Available

Role

Not Available

Physical Properties

Predicted Properties

Property	Value	Source
Water Solubility	0.64 g/L	ALOGPS
logP	2.38	ALOGPS
logP	1.98	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	4.34	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	46.53 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	49.52 m³·mol⁻¹	ChemAxon
Polarizability	18.22 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

HMDB0146617

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

26862

PDB ID

Not Available

ChEBI ID

93692

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

Showing chemical card for 3-(2-methoxyphenyl)prop-2-enoic acid (CFc000127026)

MOL for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

3D MOL for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

3D SDF for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

3D-SDF for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

PDB for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

3D PDB for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

SMILES for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

INCHI for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

Structure for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)

3D Structure for CFc000127026 (3-(2-methoxyphenyl)prop-2-enoic acid)