Tetrachlorophthalic anhydride

Odors

No information available

Receptor Interaction

No receptors available

General Information

Common Name: Tetrachlorophthalic anhydride
IUPAC Name: 4,5,6,7-tetrachloro-2-benzofuran-1,3-dione
Molecular Formula: C8Cl4O3
SMILES: C12=C(C(=C(C(=C1Cl)Cl)Cl)Cl)C(=O)OC2=O
Inchi: 1S/C8Cl4O3/c9-3-1-2(8(14)15-7(1)13)4(10)6(12)5(3)11
Inchi Key: AUHHYELHRWCWEZ-UHFFFAOYSA-N
Cas No: 117-08-8

Functional Group

Drug Likeness

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

Cross References

PubChem: 8326
Zinc: ZINC8585889
OdoRactor: View
TGSC: View

Physicochemical properties

Name Value
Molecular Weight (g/mol) 285.90
Mass (g/mol) 283.86
Molar Refractivity 56.23
Net Charge
HBD
HBA 3
Rt Bonds 0
Rings 2
TPSA 43.37
Hetero Atoms 7
Heavy Atoms 15
Aromatic Heavy Atoms 6
Melting Point (°C) 255-256.5
Boiling Point (°C@760.00mm Hg) 371
Vapor Pressure (mmHg@25.00 °C)
Vapor Density (Air =1)
Fraction Csp3 0.00
LogP 3.611
iLOGP 1.43
XLOGP3 3.80
WLOGP 3.61
MLOGP 3.92
ESOL Log S -4.30
ESOL Solubility (mg/ml) 0.014
ESOL Solubility (mol/l) 0
ESOL Class: esol_class Moderately soluble
Ali Log S -4.41
Ali Solubility (mg/ml) 0.01
Ali Solubility (mol/l) 0
Ali Class Moderately soluble
Silicos-IT LogSw -4.93
Silicos-IT Solubility (mg/ml) 0
Silicos-IT Solubility (mol/l) 0
Silicos-IT Class Moderately soluble

Pharmacokinetic profile

Name Value
GI Absorption High
BBB Permeable 1
PgP Substrate 0
Log Kp (cm/s) -5.35
Bioavailability Score 0.55
Caco2 0
Human Intestinal Absorption 1
Plasm Protein Binding 0.853
CYP1A2 Inhibitor 1
CYP2C19 Inhibitor 0
CYP2C9 Inhibitor 1
CYP2D6 inhibitor 0
CYP3A4 inhibitor 0
Ames mutagenesis 0
Acute Oral Toxicity 1.919
Carcinogenicity (Binary) 0
Carcinogenicity (Trinary) Non-required
Eye Irritation 1
Hepatotoxicity 0
Androgen Receptor Binding 0
Aromatase Binding 0
Estrogen Receptor Binding 1
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