O-ETHYL S-(2-FURYLMETHYL)THIOCARBONATE
Relevant Data
Food Additives Approved by WHO:
General Information
| Mainterm | O-ETHYL S-(2-FURYLMETHYL)THIOCARBONATE |
| Doc Type | EAF |
| CAS Reg.No.(or other ID) | 376595-42-5 |
| Regnum |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 15540144 |
| IUPAC Name | ethyl furan-2-ylmethylsulfanylformate |
| InChI | InChI=1S/C8H10O3S/c1-2-10-8(9)12-6-7-4-3-5-11-7/h3-5H,2,6H2,1H3 |
| InChI Key | RPDATXKSJBDCAP-UHFFFAOYSA-N |
| Canonical SMILES | CCOC(=O)SCC1=CC=CO1 |
| Molecular Formula | C8H10O3S |
| Wikipedia | O-ethyl S-(2-furylmethyl)thiocarbonate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 186.225 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 5 |
| Complexity | 149.0 |
| CACTVS Substructure Key Fingerprint | A A A D c c B w M A B 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 Q A A A A A C A S k 0 A K y D I A A B E i I A K h S i A A C C A A k I B A I i A E G C M g M J j K k 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 | 64.7 |
| Monoisotopic Mass | 186.035 |
| Exact Mass | 186.035 |
| XLogP3 | None |
| XLogP3-AA | 2.0 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 12 |
| 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+ | 0.9649 |
| Human Intestinal Absorption | HIA+ | 1.0000 |
| Caco-2 Permeability | Caco2+ | 0.5700 |
| P-glycoprotein Substrate | Non-substrate | 0.7400 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7424 |
| Non-inhibitor | 0.8820 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8274 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.7408 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8070 |
| CYP450 2D6 Substrate | Non-substrate | 0.8714 |
| CYP450 3A4 Substrate | Non-substrate | 0.7439 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6600 |
| CYP450 2C9 Inhibitor | Inhibitor | 0.5282 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9028 |
| CYP450 2C19 Inhibitor | Inhibitor | 0.7008 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.9365 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.7350 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8875 |
| Non-inhibitor | 0.9359 | |
| AMES Toxicity | Non AMES toxic | 0.7407 |
| Carcinogens | Non-carcinogens | 0.6617 |
| Fish Toxicity | High FHMT | 0.9311 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9753 |
| Honey Bee Toxicity | High HBT | 0.8484 |
| Biodegradation | Ready biodegradable | 0.8914 |
| Acute Oral Toxicity | III | 0.7619 |
| Carcinogenicity (Three-class) | Non-required | 0.5180 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.5290 | LogS |
| Caco-2 Permeability | 1.1052 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.4086 | LD50, mol/kg |
| Fish Toxicity | 1.5970 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.2508 | 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 - Monothioacetal - Furan - Thiocarbonic acid derivative - Carbonic acid derivative - Oxacycle - Sulfenyl compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Carbonyl group - 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