Isoxepac
Isoxepac
  • CAS No.:55453-87-7
Other grades of this product :

Isoxepac Basic information
Product Name:Isoxepac
Synonyms:Olopatadine Impurity 3(Olopatadine USP RC C);6,11-Dihydro-11-oxodibenzo[b,e]oxepin-2-acetic acid, 97.0%;e)oxepin-2-aceticacid,6,11-dihydro-11-oxo-dibenz(;hp549;DIBENZ[B,E]OXEPIN-2-ACETIC ACID, 6,11-DIOHYDRO-11-OXO;6,11-Hydro-11-Oxo-Dibenz[B,E]Oxepin-2-Acetic Acid;Olapatadine;11-Oxo-6,11-Dihydrobenz(b,e)oxepin-2-Acetic Acid (Isoxepac)
CAS:55453-87-7
MF:C16H12O4
MW:268.26
EINECS:611-268-9
Product Categories:API;Pharmaceutical intermediate;APIs Intermediate;Intermediates & Fine Chemicals;Pharmaceuticals;bc0001
Mol File:55453-87-7.mol
Isoxepac Chemical Properties
Melting point 130-132°C
Boiling point 528.2±50.0 °C(Predicted)
density 1.39 g/cm3
storage temp. Sealed in dry,Room Temperature
solubility soluble in Methanol
pka4.24±0.10(Predicted)
form neat
color White to Light yellow to Light orange
Merck 14,5237
InChIKeyQFGMXJOBTNZHEL-UHFFFAOYSA-N
CAS DataBase Reference55453-87-7(CAS DataBase Reference)
Safety Information
Hazard Codes T
Risk Statements 25-62
Safety Statements 36/37-45
RIDADR UN 2811 6.1 / PGIII
RTECS HQ4110000
HazardClass 6.1
PackingGroup III
HS Code 2932996560
ToxicityLD50 orally in rats: 199 mg/kg (Ueno)
MSDS Information
Isoxepac Usage And Synthesis
Chemical PropertiesBeige Solid
UsesIsoxepac is a non-steroidal anti-inflammatory with analgesic and antipyretic activity. It is more slowly absorbed and eliminated in the rat and rabbit after oral dosing than in the dog, rhesus monkey and man.It can be used to treat allergic rhinitis, urticaria, and skin diseases with itching symptoms.
DefinitionChEBI: Isoxepac is a dibenzooxazepine.
PreparationIsoxic acid is an important intermediate in the synthesis of the new preferred anti-allergic drug, olopatadine hydrochloride, preparation method of isoxepac:(1) condensation: prepare p-hydroxyphenylaceticacid 8-12 part, phthalide 6-12 part, sodium methylate 8-12 part by weight; Dissolve with DMAC and to add said sodium methylate behind said p-hydroxyphenylaceticacid and the phthalide; Be that 0.1-10Pa is heated to 80-170 ℃ of reaction 3-10h at pressure then; Regulate the pH value to 1-5,4-(2-carboxyl benzyloxy) toluylic acid is separated out in crystallization;(2) cyclization: with Glacial acetic acid min. 99.5 dissolving step (1) gained 4-(2-carboxyl benzyloxy) toluylic acid, adding 3-52 weight part polyphosphoric acid again, is that 0.1-10Pa is heated to 30-100 ℃ of reaction 3-12h at pressure, and crystallisation by cooling gets the Isoxepac bullion then;(3) purify: behind the said Isoxepac bullion of acetic acid ethyl dissolution, refining decolouring gets the Isoxepac product.https://patents.google.com/patent/CN102838582A/en
Brand nameArtil(Hoechst-Roussel) .
Isoxepac Preparation Products And Raw materials
Preparation ProductsOlopatadine-->6,11-dihydro-11-oxo-dibenz[b,e]oxepin-2-acetate,methyl ester

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