2-METHOXY-4-VINYLPHENOL
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | 4-HYDROXY-3-METHOXYSTYRENE, p-VINYLCATECHOL-o-METHYL ETHER, p-VINYLGUAIACOL |
| Chemical Names: | 2-METHOXY-4-VINYLPHENOL |
| CAS number: | 7786-61-0 |
| COE number: | 177 |
| JECFA number: | 725 |
| FEMA number: | 2675 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2000 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 901-JECFA 55/44 |
| Tox Monograph: | FAS 46-JECFA 55/165 |
| Specification: | COMPENDIUM ADDENDUM 8/FNP 52 Add.8/172 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 332 |
| IUPAC Name | 4-ethenyl-2-methoxyphenol |
| InChI | InChI=1S/C9H10O2/c1-3-7-4-5-8(10)9(6-7)11-2/h3-6,10H,1H2,2H3 |
| InChI Key | YOMSJEATGXXYPX-UHFFFAOYSA-N |
| Canonical SMILES | COC1=C(C=CC(=C1)C=C)O |
| Molecular Formula | C9H10O2 |
| Wikipedia | 2-methoxy-4-vinylphenol |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 150.177 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Complexity | 134.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B w M A A A A A A A A A A A A A A A A A A A A A A A A A A w A A A A A A A A A A A B A A A A G g A A C A A A D A S A m A I y B o A A B g C A A i B C A A A C C A A g I A A I i A A G i I g N J i K G M R q A c C M k w B E L u A e A w B A O I A A B A A A A Q A B A A A I A A A C A A A A A A A A A A A = = |
| Topological Polar Surface Area | 29.5 |
| Monoisotopic Mass | 150.068 |
| Exact Mass | 150.068 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 11 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
Food Additives Biosynthesis/Degradation
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.8480 |
| Human Intestinal Absorption | HIA+ | 0.9904 |
| Caco-2 Permeability | Caco2+ | 0.8788 |
| P-glycoprotein Substrate | Non-substrate | 0.6833 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7123 |
| Non-inhibitor | 0.8661 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8574 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7695 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7598 |
| CYP450 2D6 Substrate | Non-substrate | 0.7905 |
| CYP450 3A4 Substrate | Non-substrate | 0.6255 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5727 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9246 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9372 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.6716 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8655 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6534 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8946 |
| Non-inhibitor | 0.9324 | |
| AMES Toxicity | Non AMES toxic | 0.9132 |
| Carcinogens | Non-carcinogens | 0.8519 |
| Fish Toxicity | High FHMT | 0.9188 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9582 |
| Honey Bee Toxicity | High HBT | 0.8122 |
| Biodegradation | Ready biodegradable | 0.5631 |
| Acute Oral Toxicity | III | 0.8604 |
| Carcinogenicity (Three-class) | Non-required | 0.5331 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.9439 | LogS |
| Caco-2 Permeability | 1.6012 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.0980 | LD50, mol/kg |
| Fish Toxicity | 1.0940 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.5496 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Phenols |
| Subclass | Methoxyphenols |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Methoxyphenols |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Methoxyphenol - Phenoxy compound - Methoxybenzene - Styrene - Phenol ether - Anisole - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Monocyclic benzene moiety - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as methoxyphenols. These are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. |
From ClassyFire