2-THIENYLMETHANOL
Relevant Data
Food Additives Approved in the United States
General Information
CAS number: | 636-72-6 |
JECFA number: | 2111 |
FEMA number: | 4642 |
Functional Class: |
Flavouring Agent FLAVOURING_AGENT |
From apps.who.int
Evaluations
Evaluation year: | 2012 |
ADI: | No safety concern at current levels of intake when used as a flavouring agent |
Specs Code: | N |
Report: | TRS 974-JECFA 76 |
Tox Monograph: | FAS 67 JECFA 76 |
Specification: | Compendium of FAO food additive specifications |
From apps.who.int
Computed Descriptors
Download SDF2D Structure | |
CID | 69467 |
IUPAC Name | thiophen-2-ylmethanol |
InChI | InChI=1S/C5H6OS/c6-4-5-2-1-3-7-5/h1-3,6H,4H2 |
InChI Key | ZPHGMBGIFODUMF-UHFFFAOYSA-N |
Canonical SMILES | C1=CSC(=C1)CO |
Molecular Formula | C5H6OS |
Wikipedia | 2-thienylmethanol |
From Pubchem
Computed Properties
Property Name | Property Value |
---|---|
Molecular Weight | 114.162 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 2 |
Rotatable Bond Count | 1 |
Complexity | 56.0 |
CACTVS Substructure Key Fingerprint | A A A D c Y B g I 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 C A A A C A C k 0 A K w A Y A A A g i E A C B C A A A D A I A g C B B I i B g A C I g I N i K g E R C A U A A k w A E o 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 = = |
Topological Polar Surface Area | 48.5 |
Monoisotopic Mass | 114.014 |
Exact Mass | 114.014 |
Compound Is Canonicalized | True |
Formal Charge | 0 |
Heavy Atom Count | 7 |
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+ | 0.9849 |
Human Intestinal Absorption | HIA+ | 0.9878 |
Caco-2 Permeability | Caco2+ | 0.6439 |
P-glycoprotein Substrate | Non-substrate | 0.8150 |
P-glycoprotein Inhibitor | Non-inhibitor | 0.9724 |
Non-inhibitor | 0.9103 | |
Renal Organic Cation Transporter | Non-inhibitor | 0.8329 |
Distribution | ||
Subcellular localization | Mitochondria | 0.4344 |
Metabolism | ||
CYP450 2C9 Substrate | Non-substrate | 0.7052 |
CYP450 2D6 Substrate | Non-substrate | 0.8865 |
CYP450 3A4 Substrate | Non-substrate | 0.8354 |
CYP450 1A2 Inhibitor | Non-inhibitor | 0.6031 |
CYP450 2C9 Inhibitor | Non-inhibitor | 0.7821 |
CYP450 2D6 Inhibitor | Non-inhibitor | 0.8360 |
CYP450 2C19 Inhibitor | Non-inhibitor | 0.6086 |
CYP450 3A4 Inhibitor | Non-inhibitor | 0.9642 |
CYP Inhibitory Promiscuity | High CYP Inhibitory Promiscuity | 0.5000 |
Excretion | ||
Toxicity | ||
Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.9666 |
Non-inhibitor | 0.9490 | |
AMES Toxicity | Non AMES toxic | 0.8997 |
Carcinogens | Non-carcinogens | 0.6601 |
Fish Toxicity | High FHMT | 0.5426 |
Tetrahymena Pyriformis Toxicity | High TPT | 0.7182 |
Honey Bee Toxicity | High HBT | 0.7842 |
Biodegradation | Ready biodegradable | 0.8258 |
Acute Oral Toxicity | III | 0.5232 |
Carcinogenicity (Three-class) | Danger | 0.4041 |
From admetSAR
ADMET Predicted Profile --- Regression
Model | Value | Unit |
---|---|---|
Absorption | ||
Aqueous solubility | -0.6263 | LogS |
Caco-2 Permeability | 1.5232 | LogPapp, cm/s |
Distribution | ||
Metabolism | ||
Excretion | ||
Toxicity | ||
Rat Acute Toxicity | 2.4553 | LD50, mol/kg |
Fish Toxicity | 1.7777 | pLC50, mg/L |
Tetrahymena Pyriformis Toxicity | -0.3411 | 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 - Thiophene - Organic oxygen compound - Hydrocarbon derivative - Aromatic alcohol - Primary alcohol - Organooxygen compound - Alcohol - 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