ETHYL 2-METHYL-4-PENTENOATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | ETHYL 2-METHYL-4-PENTENOATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 53399-81-8 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 62024 |
| IUPAC Name | ethyl 2-methylpent-4-enoate |
| InChI | InChI=1S/C8H14O2/c1-4-6-7(3)8(9)10-5-2/h4,7H,1,5-6H2,2-3H3 |
| InChI Key | BDBGKYIBDXAVMX-UHFFFAOYSA-N |
| Canonical SMILES | CCOC(=O)C(C)CC=C |
| Molecular Formula | C8H14O2 |
| Wikipedia | ethyl 2-methyl-4-pentenoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 142.198 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 5 |
| Complexity | 118.0 |
| 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 A A A A A A A A A A A A A A A A A G g A A A A A A D Q C g g A I C C A A A B A C I A C D S C A A A A A A g A A A I A A E A A A g A A B A A A Q A C A A A E g A A A A A A A A A A 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 A A A A = = |
| Topological Polar Surface Area | 26.3 |
| Monoisotopic Mass | 142.099 |
| Exact Mass | 142.099 |
| XLogP3 | None |
| XLogP3-AA | 2.1 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 10 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| 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+ | 0.9830 |
| Human Intestinal Absorption | HIA+ | 0.9957 |
| Caco-2 Permeability | Caco2+ | 0.7331 |
| P-glycoprotein Substrate | Non-substrate | 0.7918 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8066 |
| Non-inhibitor | 0.6905 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.9063 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5146 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8818 |
| CYP450 2D6 Substrate | Non-substrate | 0.9001 |
| CYP450 3A4 Substrate | Non-substrate | 0.6771 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6721 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9115 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9395 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9112 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9302 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7875 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9639 |
| Non-inhibitor | 0.9497 | |
| AMES Toxicity | Non AMES toxic | 0.9385 |
| Carcinogens | Carcinogens | 0.7431 |
| Fish Toxicity | High FHMT | 0.9732 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9321 |
| Honey Bee Toxicity | High HBT | 0.8288 |
| Biodegradation | Ready biodegradable | 0.8933 |
| Acute Oral Toxicity | III | 0.6075 |
| Carcinogenicity (Three-class) | Non-required | 0.5837 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.7005 | LogS |
| Caco-2 Permeability | 1.2628 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4799 | LD50, mol/kg |
| Fish Toxicity | 0.4301 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.1706 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty acid esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty acid esters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. |
From ClassyFire