METHYL 2-METHYL-3-FURYL DISULFIDE
Relevant Data
Food Additives Approved in the United States
Flavouring Substances Approved by European Union:
General Information
| Synonyms: | 2-METHYL-3-FURYL METHYL DISULFIDE, 2-METHYL-3-(METHYLDITHIO)FURAN |
| Chemical Names: | METHYL 2-METHYL-3-FURYL DISULFIDE |
| CAS number: | 65505-17-1 |
| COE number: | 11924 |
| JECFA number: | 1064 |
| FEMA number: | 3573 |
| Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
| Evaluation year: | 2002 |
| ADI: | No safety concern at current levels of intake when used as a flavouring agent |
| Report: | TRS 913-JECFA 59/81 |
| Tox Monograph: | FAS 50-JECFA 59/299 |
| Specification: | COMPENDIUM ADDENDUM 10/FNP 52 Add.10/66 |
From apps.who.int
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 47649 |
| IUPAC Name | 2-methyl-3-(methyldisulfanyl)furan |
| InChI | InChI=1S/C6H8OS2/c1-5-6(9-8-2)3-4-7-5/h3-4H,1-2H3 |
| InChI Key | SRUTWBWLFKSTIS-UHFFFAOYSA-N |
| Canonical SMILES | CC1=C(C=CO1)SSC |
| Molecular Formula | C6H8OS2 |
| Wikipedia | methyl 2-methyl-3-furyl disulfide |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 160.249 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 2 |
| Complexity | 87.1 |
| CACTVS Substructure Key Fingerprint | A A A D c c B g I A B g 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 g 0 A K y B Y A A B E C I A K h S g A A G C A A k I A A I i B s G C M g M J j K E N B 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 | 63.7 |
| Monoisotopic Mass | 160.002 |
| Exact Mass | 160.002 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 9 |
| 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+ | 0.9911 |
| Human Intestinal Absorption | HIA+ | 0.9874 |
| Caco-2 Permeability | Caco2+ | 0.5957 |
| P-glycoprotein Substrate | Non-substrate | 0.7918 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7942 |
| Non-inhibitor | 0.9471 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8323 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.4626 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.7887 |
| CYP450 2D6 Substrate | Non-substrate | 0.8239 |
| CYP450 3A4 Substrate | Non-substrate | 0.7027 |
| CYP450 1A2 Inhibitor | Inhibitor | 0.6576 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.5646 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.8481 |
| CYP450 2C19 Inhibitor | Inhibitor | 0.6012 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8807 |
| CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.8103 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9344 |
| Non-inhibitor | 0.9285 | |
| AMES Toxicity | Non AMES toxic | 0.7740 |
| Carcinogens | Non-carcinogens | 0.6990 |
| Fish Toxicity | High FHMT | 0.5162 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.5212 |
| Honey Bee Toxicity | High HBT | 0.7864 |
| Biodegradation | Not ready biodegradable | 0.6662 |
| Acute Oral Toxicity | II | 0.5472 |
| Carcinogenicity (Three-class) | Non-required | 0.4082 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -2.2887 | LogS |
| Caco-2 Permeability | 1.6426 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 2.6016 | LD50, mol/kg |
| Fish Toxicity | 1.6802 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | -0.0922 | 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 - Organic disulfide - Oxacycle - Sulfenyl compound - Organic oxygen compound - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - 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