(Z)-Hex-3-enyl benzoate
Relevant Data
Food Additives Approved in the United States:
Food Additives Approved by WHO:
General Information
| Chemical name | (Z)-Hex-3-enyl benzoate |
| CAS number | 25152-85-6 |
| COE number | 11778 |
| JECFA number | 858 |
| Flavouring type | substances |
| FL No. | 09.806 |
| Mixture | No |
| Purity of the named substance at least 95% unless otherwise specified | 93-97% cis-hexenyl benzoate; 1-2% trans-3-hexenyl benzoate |
| Reference body | EFSA |
From webgate.ec.europa.eu
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 5367706 |
| IUPAC Name | [(Z)-hex-3-enyl] benzoate |
| InChI | InChI=1S/C13H16O2/c1-2-3-4-8-11-15-13(14)12-9-6-5-7-10-12/h3-7,9-10H,2,8,11H2,1H3/b4-3- |
| InChI Key | BCOXBEHFBZOJJZ-ARJAWSKDSA-N |
| Canonical SMILES | CCC=CCCOC(=O)C1=CC=CC=C1 |
| Molecular Formula | C13H16O2 |
| Wikipedia | (3Z)-3-hexenyl benzoate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 204.269 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 6 |
| Complexity | 203.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e 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 k A A A I i A E A C M g I J j K A N R i C M Q A k w A E I q Y e I y C 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 | 204.115 |
| Exact Mass | 204.115 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 15 |
| 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+ | 0.9721 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.8009 |
| P-glycoprotein Substrate | Non-substrate | 0.6666 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.8623 |
| Non-inhibitor | 0.8510 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.7971 |
| Distribution | ||
| Subcellular localization | Plasma membrane | 0.6423 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8175 |
| CYP450 2D6 Substrate | Non-substrate | 0.9080 |
| CYP450 3A4 Substrate | Non-substrate | 0.6555 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6202 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8750 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8910 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8059 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9372 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.5320 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7838 |
| Non-inhibitor | 0.8590 | |
| AMES Toxicity | Non AMES toxic | 0.8390 |
| Carcinogens | Non-carcinogens | 0.6987 |
| Fish Toxicity | High FHMT | 0.9446 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9997 |
| Honey Bee Toxicity | High HBT | 0.7216 |
| Biodegradation | Ready biodegradable | 0.7912 |
| Acute Oral Toxicity | III | 0.9144 |
| Carcinogenicity (Three-class) | Non-required | 0.5923 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.9530 | LogS |
| Caco-2 Permeability | 1.4728 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.6424 | LD50, mol/kg |
| Fish Toxicity | 0.8540 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.7223 | 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 - 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