2-Methoxynaphthalene
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | 2-Methoxynaphthalene |
| CAS number | 93-04-9 |
| JECFA number | 1257 |
| Flavouring type | substances |
| FL No. | 04.074 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 7119 |
| IUPAC Name | 2-methoxynaphthalene |
| InChI | InChI=1S/C11H10O/c1-12-11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3 |
| InChI Key | LUZDYPLAQQGJEA-UHFFFAOYSA-N |
| Canonical SMILES | COC1=CC2=CC=CC=C2C=C1 |
| Molecular Formula | C11H10O |
| Wikipedia | β-naphthyl methyl ether |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 158.2 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Complexity | 144.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B w I 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 Y A A A A A A A A A D B U A A A G g A A A A A A D A S A m A I y B s A A B A C A A i B C A A A C C A A g I A A I i A A G C I g M J i K E M R q A M C A k w B E I q A e A w L A O o A A B A A A Q A A B A A A I A A C A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 9.2 |
| Monoisotopic Mass | 158.073 |
| Exact Mass | 158.073 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 12 |
| 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+ | 0.9344 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8829 |
| P-glycoprotein Substrate | Non-substrate | 0.6240 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7812 |
| Non-inhibitor | 0.8214 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7763 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5252 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7483 |
| CYP450 2D6 Substrate | Non-substrate | 0.8070 |
| CYP450 3A4 Substrate | Non-substrate | 0.5773 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.9794 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.6588 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8960 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.5000 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8786 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.5281 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7885 |
| Non-inhibitor | 0.8444 | |
| AMES Toxicity | AMES toxic | 0.9154 |
| Carcinogens | Non-carcinogens | 0.8679 |
| Fish Toxicity | High FHMT | 0.9217 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9823 |
| Honey Bee Toxicity | High HBT | 0.8914 |
| Biodegradation | Not ready biodegradable | 0.8472 |
| Acute Oral Toxicity | III | 0.8234 |
| Carcinogenicity (Three-class) | Warning | 0.5310 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -4.3774 | LogS |
| Caco-2 Permeability | 1.5755 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.5316 | LD50, mol/kg |
| Fish Toxicity | 0.9591 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 1.0096 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Naphthalenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthalenes |
| Alternative Parents | |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Naphthalene - Anisole - Alkyl aryl ether - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings. |
From ClassyFire