CAS 28291-63-6

Fórmula: C16H13NO2

InChI: InChI=1S/C16H13NO2/c1-11(18)17-14-8-4-2-6-12(14)10-16(19)13-7-3-5-9-15(13)17/h2-9H,10H2,1H3

Clave InChI: BVFWPQQJWYTKGK-UHFFFAOYSA-N

SMILES: CC(=O)N1C2=CC=CC=C2CC(=O)C3=CC=CC=C31

5-Acetyl-5H-dibenzo[b,f]azepin-10(11H)-one

CAS: 28291-63-6

Fórmula: C₁₆H₁₃NO₂

Peso molecular: 251.2799

Ref: IN-DA00C2TD

Oxcarbazepine Impurity 11

CAS: 28291-63-6

Fórmula: C₁₆H₁₃NO₂

Peso molecular: 251.29

Ref: 4Z-O-0637

5-Acetyl-5,11-dihydro-10H-dibenz[b,f]azepin-10-one

Producto controlado

CAS: 28291-63-6

Applications Impurity of Oxcarbazepine (O869250), an anticonvulsant and metabolite of Eslicarbazepine acetate, (BIA 2-093), a novel central nervous system drug.
References Thomas, S., et al.: J. Pharma. Biomed. Anal., 61, 165 (2012); Bhattacharjee, A.K., et al.: J. Chem. Info. Comp. Sci., 42, 1212 (2002);

Fórmula: C₁₆H₁₃NO₂

Forma y color: Neat

Peso molecular: 251.28

Ref: TR-A179120

5-Acetyl-5,11-dihydro-10H-dibenz[b,f]azepin-10-one

CAS: 28291-63-6

5-Acetyl-5,11-dihydro-10H-dibenz[b,f]azepin-10-one is a synthetic compound that belongs to the class of azepinones. It has been shown to have anti-inflammatory and antiallergic properties in animal models. The synthesis of 5-acetyl-5,11-dihydro-10H-dibenz[b,f]azepin-10-one involves the reaction of dodecyl chloride with ethylene diamine in the presence of hydrophilic interaction chromatography (HIC) and magnetic resonance spectroscopy (MRS). This process leads to the formation of an azepinone product.

Fórmula: C₁₆H₁₃NO₂

Pureza: Min. 95%

Peso molecular: 251.28 g/mol

Ref: 3D-DBA29163

Carbamazepine Impurity 8

CAS: 28291-63-6

Fórmula: C₁₆H₁₃NO₂

Peso molecular: 251.28

Ref: ST-EA-CP-C8023