4-ALLYL-2,6-DIMETHOXYPHENOL
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
Synonyms: | 4-ALLYLSYRINGOL, 2,6-DIMETHOXY-4-(2-PROPENYL)PHENOL, 6-METHOXY EUGENOL |
Chemical Names: | 4-ALLYL-2,6-DIMETHOXYPHENOL |
CAS number: | 6627-88-9 |
COE number: | 11214 |
JECFA number: | 726 |
FEMA number: | 3655 |
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 9/FNP 52 Add.9/124 (2001) |
From apps.who.int
Computed Descriptors
Download SDF2D Structure | |
CID | 226486 |
IUPAC Name | 2,6-dimethoxy-4-prop-2-enylphenol |
InChI | InChI=1S/C11H14O3/c1-4-5-8-6-9(13-2)11(12)10(7-8)14-3/h4,6-7,12H,1,5H2,2-3H3 |
InChI Key | FWMPKHMKIJDEMJ-UHFFFAOYSA-N |
Canonical SMILES | COC1=CC(=CC(=C1O)OC)CC=C |
Molecular Formula | C11H14O3 |
Wikipedia | 4-allyl-2,6-dimethoxyphenol |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 194.23 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 3 |
Rotatable Bond Count | 4 |
Complexity | 167.0 |
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 y K G M R q A c C M l w B U L u A e A 4 L w O I A A B C A A A Q A B A A A I Q A A C A A A A A A A A A A A = = |
Topological Polar Surface Area | 38.7 |
Monoisotopic Mass | 194.094 |
Exact Mass | 194.094 |
XLogP3 | None |
XLogP3-AA | 2.6 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 14 |
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
ADMET Predicted Profile --- Classification
Model | Result | Probability |
---|---|---|
Absorption | ||
Blood-Brain Barrier | BBB+ | 0.8665 |
Human Intestinal Absorption | HIA+ | 0.9830 |
Caco-2 Permeability | Caco2+ | 0.8429 |
P-glycoprotein Substrate | Non-substrate | 0.6399 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.5986 |
Non-inhibitor | 0.5896 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8705 |
Distribution | ||
Subcellular localization | Mitochondria | 0.7978 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.8068 |
CYP450 2D6 Substrate | Non-substrate | 0.8219 |
CYP450 3A4 Substrate | Non-substrate | 0.6303 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.5552 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.9487 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.8761 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.5090 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.6694 |
CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.5128 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9101 |
Non-inhibitor | 0.9527 | |
AMES Toxicity | Non AMES toxic | 0.8779 |
Carcinogens | Non-carcinogens | 0.8200 |
Fish Toxicity | High FHMT | 0.9582 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.9692 |
Honey Bee Toxicity | High HBT | 0.8272 |
Biodegradation | Not ready biodegradable | 0.8395 |
Acute Oral Toxicity | III | 0.8439 |
Carcinogenicity (Three-class) | Non-required | 0.6545 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -2.3137 | LogS |
Caco-2 Permeability | 1.3548 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.3677 | LD50, mol/kg |
Fish Toxicity | 0.8172 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | 0.5882 | 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 | M-dimethoxybenzene - Dimethoxybenzene - Methoxyphenol - Phenoxy compound - Methoxybenzene - Phenol ether - Anisole - 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