METHYL PHENYLACETATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | METHYL PHENYLACETATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 101-41-7 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 7559 |
| IUPAC Name | methyl 2-phenylacetate |
| InChI | InChI=1S/C9H10O2/c1-11-9(10)7-8-5-3-2-4-6-8/h2-6H,7H2,1H3 |
| InChI Key | CRZQGDNQQAALAY-UHFFFAOYSA-N |
| Canonical SMILES | COC(=O)CC1=CC=CC=C1 |
| Molecular Formula | C9H10O2 |
| Wikipedia | methyl phenylacetate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 150.177 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Complexity | 126.0 |
| 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 A A A A D A C A m A I y C I A A B A C I A i D S C A A C A A A g A A A I i A E A A I g I I D K A F R C A I A A k w A E I i A e I y K C O 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 A A A A = = |
| Topological Polar Surface Area | 26.3 |
| 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
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9760 |
| Human Intestinal Absorption | HIA+ | 0.9909 |
| Caco-2 Permeability | Caco2+ | 0.8528 |
| P-glycoprotein Substrate | Non-substrate | 0.7359 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9438 |
| Non-inhibitor | 0.9768 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8446 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6925 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7750 |
| CYP450 2D6 Substrate | Non-substrate | 0.9262 |
| CYP450 3A4 Substrate | Non-substrate | 0.7430 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.5288 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9678 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9506 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9269 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9861 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9019 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9382 |
| Non-inhibitor | 0.9782 | |
| AMES Toxicity | Non AMES toxic | 0.9776 |
| Carcinogens | Non-carcinogens | 0.6566 |
| Fish Toxicity | High FHMT | 0.8726 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9682 |
| Honey Bee Toxicity | High HBT | 0.7610 |
| Biodegradation | Ready biodegradable | 0.7309 |
| Acute Oral Toxicity | III | 0.8419 |
| Carcinogenicity (Three-class) | Non-required | 0.7147 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.4105 | LogS |
| Caco-2 Permeability | 1.5594 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7961 | LD50, mol/kg |
| Fish Toxicity | 1.1440 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.1178 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzene and substituted derivatives |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Monocyclic benzene moiety - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. |
From ClassyFire