O-Ethyl S-(2-furylmethyl)thiocarbonate

Odors

Receptor Interaction

No receptors available

Odor Profile

Strength: high

General Information

Common Name: O-Ethyl S-(2-furylmethyl)thiocarbonate
IUPAC Name: ethyl furan-2-ylmethylsulfanylformate
Molecular Formula: C6H11NO2S
SMILES: CCOC(=O)SCC1=CC=CO1
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
Cas No: 376595-42-5

Functional Group

Esters
Furan
Thioesters

Drug Likeness

Name Value
Lipinski Violations 0
Ghose Violations 0
Veber Violations 0
Egan Violations 0
Muegge Violations 1

Cross References

PubChem: 15540144
Zinc: ZINC34579674
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 161.22
Mass (g/mol) 186.035
Molar Refractivity 41.75
Net Charge
HBD 1
HBA 2
Rt Bonds 5
Rings 1
TPSA 71.47
Hetero Atoms 4
Heavy Atoms 10
Aromatic Heavy Atoms 0
Melting Point (°C)
Boiling Point (°C@760.00mm Hg) 130.00 to 135.00
Vapor Pressure (mmHg@25.00 °C)
Vapor Density (Air =1)
Fraction Csp3 0.67
LogP 2.669
iLOGP 1.73
XLOGP3 0.37
WLOGP 0.40
MLOGP -0.12
ESOL Log S -0.74
ESOL Solubility (mg/ml) 29.2
ESOL Solubility (mol/l) 0.181
ESOL Class: esol_class Very soluble
Ali Log S -1.44
Ali Solubility (mg/ml) 5.91
Ali Solubility (mol/l) 0.04
Ali Class Very soluble
Silicos-IT LogSw -1.51
Silicos-IT Solubility (mg/ml) 4.95
Silicos-IT Solubility (mol/l) 0.03
Silicos-IT Class Soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 0
PgP Substrate 0
Log Kp (cm/s) -7.02
Bioavailability Score 0.55
Caco2 1
Human Intestinal Absorption 1
Plasm Protein Binding 0.79
CYP1A2 Inhibitor 0
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 0
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.901
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Non-required
Eye Irritation 1
Hepatotoxicity 0
Androgen Receptor Binding 0
Aromatase Binding 0
Estrogen Receptor Binding 0
Glucocorticoid Receptor Binding 0
Thyroid Receptor Binding 0
BRCP inhibitor 0
BSEP inhibitor 0
OATP1B1 inhibitor 1
OATP1B3 inhibitor 1
OATP2B1 inhibitor 0
OCT1 inhibitor 0
OCT2 inhibitor 0