CIS-3-HEXENYL ACETOACETATE
Relevant Data
Food Additives Approved by WHO:
General Information
| Mainterm | CIS-3-HEXENYL ACETOACETATE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 84434-20-8 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 20836219 |
| IUPAC Name | [(Z)-hex-3-enyl] 3-oxobutanoate |
| InChI | InChI=1S/C10H16O3/c1-3-4-5-6-7-13-10(12)8-9(2)11/h4-5H,3,6-8H2,1-2H3/b5-4- |
| InChI Key | JCPGKFSGEPVXMI-PLNGDYQASA-N |
| Canonical SMILES | CCC=CCCOC(=O)CC(=O)C |
| Molecular Formula | C10H16O3 |
| Wikipedia | (3Z)-hexenyl acetoacetate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 184.235 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 7 |
| Complexity | 194.0 |
| 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 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 C A S g g A I C C A A A B A C I A K D S C A A A A A A g A A A I C A E A A A g A A B Q I A Q A C A A A E Y A A I 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 A A A A A = = |
| Topological Polar Surface Area | 43.4 |
| Monoisotopic Mass | 184.11 |
| Exact Mass | 184.11 |
| 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+ | 0.9799 |
| Human Intestinal Absorption | HIA+ | 0.9964 |
| Caco-2 Permeability | Caco2+ | 0.6939 |
| P-glycoprotein Substrate | Non-substrate | 0.6883 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.6819 |
| Non-inhibitor | 0.5905 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8831 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7317 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8886 |
| CYP450 2D6 Substrate | Non-substrate | 0.8935 |
| CYP450 3A4 Substrate | Non-substrate | 0.6055 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6675 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.8869 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9160 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.8660 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8899 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.6909 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8814 |
| Non-inhibitor | 0.8912 | |
| AMES Toxicity | Non AMES toxic | 0.9181 |
| Carcinogens | Carcinogens | 0.5292 |
| Fish Toxicity | High FHMT | 0.8809 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9949 |
| Honey Bee Toxicity | High HBT | 0.7708 |
| Biodegradation | Ready biodegradable | 0.9419 |
| Acute Oral Toxicity | II | 0.6480 |
| Carcinogenicity (Three-class) | Non-required | 0.5637 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.1189 | LogS |
| Caco-2 Permeability | 0.8962 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.9413 | LD50, mol/kg |
| Fish Toxicity | 0.4836 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.4303 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Class | Keto acids and derivatives |
| Subclass | Beta-keto acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Beta-keto acids and derivatives |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty acid ester - Beta-keto acid - Fatty acyl - 1,3-dicarbonyl compound - Ketone - 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 beta-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the C3 carbon atom. |
From ClassyFire