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Diclofenac EP Impurity E

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Category Human immunodeficiency Virus (HIV)
CAS 59-48-3
Description Diclofenac EP Impurity E is an impurity of Diclofenac, which is a non-selective COX inhibitor used as a non-steroidal anti-inflammatory drug (NSAID).
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Product Information

Synonyms Diclofenac sodium EP impurity E; Diclofenac potassium EP impurity E; 1,3-dihydro-2H-indol-2-one; 2H-Indol-2-one, 1,3-dihydro-; 1,3-Dihydro-2H-indol-2-one; 2-Indolinone; Oxindole; 2,3-Dihydro-1H-indol-2-one; 2-Indolone; 2-Oxindole; 2-Oxo-2,3-dihydroindole; 2-Oxoindole; 2-Oxoindoline; Indol-2(3H)-one; Indoline-2-one; NSC 274863; Oxindol
IUPAC Name 1,3-dihydroindol-2-one
Molecular Weight 133.15
Molecular Formula C8H7NO
Canonical SMILES C1C2=CC=CC=C2NC1=O
InChI InChI=1S/C8H7NO/c10-8-5-6-3-1-2-4-7(6)9-8/h1-4H,5H2,(H,9,10)
InChIKey JYGFTBXVXVMTGB-UHFFFAOYSA-N
Boiling Point 227°C
Melting Point 128°C
Flash Point 190.0±18.0 °C
Purity ≥95%
Density 1.198±0.06 g/cm3
Solubility Soluble in Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
Appearance Light Brown to Brown Solid
Storage Store at 2-8°C for short term (days to weeks) or -20°C for long term (months to years)
Complexity 155
Exact Mass 133.052763847
Index Of Refraction 1.640
In Vitro Oxindole (Indolin-2-one) is a bicyclic structure consisting of a benzene ring fused to 2-pyrrolidone. Substituted indolinones can be referred as 'privileged structures' owing to their excellent binding affinity for many receptors and to the number of approved drugs containing this scaffold. Oxindole has been found in tissues and fluids of mammals as well as natural products produced by a range of plants, bacteria and invertebrates. 2-indolinone derivatives possess diverse range of pharmacological activities including anti-cancer, anti-HIV, anti-diabetic, antibacterial, antioxidant, kinase inhibitory, AChE inhibitory, anti-leishmanial, b3 adrenergic receptor agonistic, phosphatase inhibitory, analgesic, spermicidal, vasopressin antagonists, progesterone antagonists, neuroprotection, NMDA blocker and sleep inducing activities.
PSA 29.10000
Target HIV
Vapor Pressure 0.0±0.7 mmHg at 25°C
XLogP3-AA 1.2

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