Cinnamyl acetate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | Cinnamyl acetate |
| CAS number | 103-54-8 |
| COE number | 208 |
| JECFA number | 650 |
| Flavouring type | substances |
| FL No. | 09.018 |
| 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 | 5282110 |
| IUPAC Name | [(E)-3-phenylprop-2-enyl] acetate |
| InChI | InChI=1S/C11H12O2/c1-10(12)13-9-5-8-11-6-3-2-4-7-11/h2-8H,9H2,1H3/b8-5+ |
| InChI Key | WJSDHUCWMSHDCR-VMPITWQZSA-N |
| Canonical SMILES | CC(=O)OCC=CC1=CC=CC=C1 |
| Molecular Formula | C11H12O2 |
| Wikipedia | cinnamyl acetate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 176.215 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 4 |
| Complexity | 179.0 |
| 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 g 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 A A A I g I J C K A M R C C M A A g g A A I q A c A g A A 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 | 176.084 |
| Exact Mass | 176.084 |
| XLogP3 | None |
| XLogP3-AA | 2.3 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 13 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| 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+ | 0.9803 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8627 |
| P-glycoprotein Substrate | Non-substrate | 0.7028 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.9393 |
| Non-inhibitor | 0.9184 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8128 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.6569 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7492 |
| CYP450 2D6 Substrate | Non-substrate | 0.9222 |
| CYP450 3A4 Substrate | Non-substrate | 0.7375 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.7242 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9139 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9373 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8079 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9682 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6726 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9475 |
| Non-inhibitor | 0.9788 | |
| AMES Toxicity | Non AMES toxic | 0.6958 |
| Carcinogens | Non-carcinogens | 0.6061 |
| Fish Toxicity | High FHMT | 0.9698 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9988 |
| Honey Bee Toxicity | High HBT | 0.7975 |
| Biodegradation | Ready biodegradable | 0.7845 |
| Acute Oral Toxicity | III | 0.9005 |
| Carcinogenicity (Three-class) | Non-required | 0.7360 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.1637 | LogS |
| Caco-2 Permeability | 1.6888 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6965 | LD50, mol/kg |
| Fish Toxicity | 0.3653 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.4910 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Styrenes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Styrenes |
| Alternative Parents | |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Styrene - 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 styrenes. These are organic compounds containing an ethenylbenzene moiety. |
From ClassyFire