CAS 4504-87-4

Dibenz[b,e]oxepin-11(6H)-one

Description:

Dibenz[b,e]oxepin-11(6H)-one, with the CAS number 4504-87-4, is a polycyclic aromatic compound characterized by its unique fused ring structure, which includes both benzene and oxepin moieties. This compound typically exhibits a solid state at room temperature and is known for its stability under various conditions. It is often utilized in organic synthesis and may serve as an intermediate in the production of pharmaceuticals and other chemical products. The presence of the oxepin ring contributes to its reactivity, allowing for various chemical transformations. Additionally, dibenz[b,e]oxepin-11(6H)-one may exhibit interesting biological activities, making it a subject of interest in medicinal chemistry. Its solubility can vary depending on the solvent, and it may display fluorescence properties, which can be advantageous in certain applications. Overall, dibenz[b,e]oxepin-11(6H)-one is a versatile compound with potential applications in both research and industry.

Formula: C₁₄H₁₀O₂

InChI: InChI=1/C14H10O2/c15-14-11-6-2-1-5-10(11)9-16-13-8-4-3-7-12(13)14/h1-8H,9H2

InChI key: InChIKey=YUSHFLBKQQILNV-UHFFFAOYSA-N

SMILES: O=C1C=2C(COC=3C1=CC=CC3)=CC=CC2

Synonyms:

• 6,11-Dihydrodibenz[b.e]Oxepin-11-one
• 6,11-Dihydrobenz[b,e]oxepin-11-one
• Dibenzo[B,E]Oxepin-11(6H)-One
• Dibenz[B,E]Oxepin-11(6H)-One
• Doxepinone
• 11-Oxo-6,11-Dihydrodibenzo[B,E]Oxepin
• 11-Dihydrodibenz[B,E]Oxepin-11-One
• 6H-Dibenzo[B,E]Oxepin-11-One
• Doxepin
• 6H-Dibenzo oxepin 11 one
• 6,11-DIHYDRODIBENZO[B,E]OXEPIN-11-ONE
• 11-Oxo-6,11-dihydrodibenzo oxepin

Doxepin impurity standard

CAS: 1225-56-5, 1229-29-4, 4504-87-4, 4504-88-5

Doxepin impurity standard

Color and Shape: White

Ref: 47-823

Doxepin Related Compound A (dibenzo[b,e]oxepin-11(6H)-one)

CAS: 4504-87-4

Aromatic heterocyclic compounds with oxygen hetero-atom(s) only, nesoi

Formula: C₁₄H₁₀O₂

Color and Shape: Beige Powder

Molecular weight: 210.06808

Ref: 45-1225511

9-oxatricyclo[9.4.0.0^{3,8}]pentadeca-1(11),3,5,7,12,14-hexaen-2-one

CAS: 4504-87-4

Formula: C₁₄H₁₀O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 210.2280

Ref: IN-DA00I8HI

Dibenzo[b,e]oxepin-11(6H)-one

CAS: 4504-87-4

Dibenzo[b,e]oxepin-11(6H)-one

Purity: 98%

Molecular weight: 210.23g/mol

Ref: 54-OR96016

Doxepin EP Impurity A (Doxepin USP Related Compound A

CAS: 4504-87-4

Formula: C₁₄H₁₀O₂

Molecular weight: 210.23

Ref: 4Z-D-154

Doxepin EP Impurity A

Controlled Product

CAS: 4504-87-4

Formula: C₁₄H₁₀O₂

Color and Shape: Neat

Molecular weight: 210.23

Ref: 86-MM0032.03

Dibenz[b,e]oxepin-11(6H)-one

Controlled Product

CAS: 4504-87-4

Applications Doxepin intermediate. A photodecomposition product of Doxepin.
References Yoshioka, T., et al.: J. Med. Chem., et al.: 21, 633 (1978), Tammilehto, S., et al.: J. Chromatography, 246, 308 (1982),

Formula: C₁₄H₁₀O₂

Color and Shape: Off-White To Light Yellow

Molecular weight: 210.23

Ref: TR-D416925

Dibenzo[b,e]oxepin-11(6H)-one

CAS: 4504-87-4

Formula: C₁₄H₁₀O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 210.232

Ref: 10-F215719

Doxepin EP impurity A

CAS: 4504-87-4

Formula: C₁₄H₁₀O₂

Molecular weight: 210.2

Ref: ST-EA-CP-D58002

Dibenz[b,e]oxepin-11(6H)-one

CAS: 4504-87-4

Dibenz[b,e]oxepin-11(6H)-one is a chemical compound that has been isolated from the endophytic fungus Microsporum canis. The compound is a nucleophilic and has shown to have anthelmintic properties. Dibenz[b,e]oxepin-11(6H)-one was synthesized by reacting doxepin hydrochloride with hydrochloric acid in the presence of matrix metalloproteinase (MMP). It has been shown to inhibit MMP activity and chloride ion uptake in mammalian cells. Dibenz[b,e]oxepin-11(6H)-one also inhibits the growth of C. elegans mutant strain that lacks dihedral symmetry.

Formula: C₁₄H₁₀O₂

Purity: Min. 95%

Molecular weight: 210.23 g/mol

Ref: 3D-FD21522