2-FURFURYLIDENEBUTYRALDEHYDE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | 2-FURFURYLIDENEBUTYRALDEHYDE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 770-27-4 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 61210 |
| IUPAC Name | 2-(furan-2-ylmethylidene)butanal |
| InChI | InChI=1S/C9H10O2/c1-2-8(7-10)6-9-4-3-5-11-9/h3-7H,2H2,1H3 |
| InChI Key | UCPFCQBLYDXPTR-UHFFFAOYSA-N |
| Canonical SMILES | CCC(=CC1=CC=CO1)C=O |
| Molecular Formula | C9H10O2 |
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 | 3 |
| Complexity | 161.0 |
| 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 S A A A A A A A A A A A A A A A A A B g A A A G g A A A A A A D A S g k A I y B I A A B E C I A q h S g A A C C A A k I A A I i A E G C M g M J j K E N R q C G S C k w B E I q Y 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 = = |
| Topological Polar Surface Area | 30.2 |
| 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 | 1 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9658 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.7031 |
| P-glycoprotein Substrate | Non-substrate | 0.6392 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.5909 |
| Non-inhibitor | 0.6931 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8535 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.4979 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8194 |
| CYP450 2D6 Substrate | Non-substrate | 0.9139 |
| CYP450 3A4 Substrate | Non-substrate | 0.7153 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.5757 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.6474 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9233 |
| CYP450 2C19 Inhibitor | Inhibitor | 0.5859 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9494 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.8522 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.7777 |
| Non-inhibitor | 0.9529 | |
| AMES Toxicity | Non AMES toxic | 0.7789 |
| Carcinogens | Non-carcinogens | 0.6248 |
| Fish Toxicity | Low FHMT | 0.5674 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9983 |
| Honey Bee Toxicity | High HBT | 0.8152 |
| Biodegradation | Ready biodegradable | 0.9054 |
| Acute Oral Toxicity | III | 0.9415 |
| Carcinogenicity (Three-class) | Warning | 0.4341 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -1.8370 | LogS |
| Caco-2 Permeability | 1.5723 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.9535 | LD50, mol/kg |
| Fish Toxicity | 0.7582 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.5051 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Heteroaromatic compounds |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Heteroaromatic compounds |
| Alternative Parents | |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Heteroaromatic compound - Furan - Enal - Alpha,beta-unsaturated aldehyde - Oxacycle - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aldehyde - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as heteroaromatic compounds. These are compounds containing an aromatic ring where a carbon atom is linked to an hetero atom. |
From ClassyFire