Methyl 4-methylbenzoate
General Information
| Chemical name | Methyl 4-methylbenzoate |
| CAS number | 99-75-2 |
| Flavouring type | substances |
| FL No. | 09.631 |
| 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 | 7455 |
| IUPAC Name | methyl 4-methylbenzoate |
| InChI | InChI=1S/C9H10O2/c1-7-3-5-8(6-4-7)9(10)11-2/h3-6H,1-2H3 |
| InChI Key | QSSJZLPUHJDYKF-UHFFFAOYSA-N |
| Canonical SMILES | CC1=CC=C(C=C1)C(=O)OC |
| Molecular Formula | C9H10O2 |
| Wikipedia | methyl 4-methylbenzoate |
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 | 2 |
| Complexity | 135.0 |
| 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 k A A A I i A E A C M g I J j K A N R i A M Q A k w A E I q Y e I y D C O Q A A A A A A A A A C 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+ | 0.9697 |
| Human Intestinal Absorption | HIA+ | 0.9938 |
| Caco-2 Permeability | Caco2+ | 0.8928 |
| P-glycoprotein Substrate | Non-substrate | 0.7918 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9666 |
| Non-inhibitor | 0.9687 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8894 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7774 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8204 |
| CYP450 2D6 Substrate | Non-substrate | 0.9409 |
| CYP450 3A4 Substrate | Non-substrate | 0.7248 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6335 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9700 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9670 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9641 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9855 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.9033 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9705 |
| Non-inhibitor | 0.9813 | |
| AMES Toxicity | Non AMES toxic | 0.9728 |
| Carcinogens | Non-carcinogens | 0.5807 |
| Fish Toxicity | High FHMT | 0.7405 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9512 |
| Honey Bee Toxicity | High HBT | 0.8021 |
| Biodegradation | Ready biodegradable | 0.8079 |
| Acute Oral Toxicity | III | 0.9188 |
| Carcinogenicity (Three-class) | Non-required | 0.7051 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.0204 | LogS |
| Caco-2 Permeability | 1.8179 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.7551 | LD50, mol/kg |
| Fish Toxicity | 2.0806 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.2805 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Benzoic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Benzoic acid esters |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Benzoate ester - Benzoyl - Toluene - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. |
From ClassyFire