CAS 2039-77-2

9-Acetylphenanthrene

Description:

9-Acetylphenanthrene is an organic compound characterized by its structure, which consists of a phenanthrene backbone with an acetyl group attached at the 9-position. This compound is typically a yellow to brown solid at room temperature and is known for its aromatic properties due to the presence of multiple fused benzene rings. It is relatively insoluble in water but soluble in organic solvents such as ethanol and acetone. 9-Acetylphenanthrene can undergo various chemical reactions, including electrophilic substitution and reduction, making it useful in organic synthesis and as an intermediate in the production of dyes and pharmaceuticals. Additionally, it exhibits fluorescence, which can be exploited in various applications, including materials science and photonics. Safety data indicates that, like many aromatic compounds, it should be handled with care due to potential health risks associated with exposure. Overall, 9-acetylphenanthrene is a significant compound in organic chemistry with various applications in research and industry.

Formula: C₁₆H₁₂O

InChI: InChI=1S/C16H12O/c1-11(17)16-10-12-6-2-3-7-13(12)14-8-4-5-9-15(14)16/h2-10H,1H3

InChI key: InChIKey=UIFAWZBYTTXSOG-UHFFFAOYSA-N

SMILES: C(C)(=O)C1=C2C(=C3C(=C1)C=CC=C3)C=CC=C2

Synonyms:

• 1-(9-Phenanthrenyl)ethanone
• 1-(Phenanthren-9-Yl)Ethanone
• Ethanone, 1-(9-phenanthrenyl)-
• Ketone, methyl 9-phenanthryl
• Methyl 9-Phenanthryl Ketone
• NSC 15306
• NSC 231776
• 9-Acetylphenanthrene

Ethanone, 1-(9-phenanthrenyl)-

CAS: 2039-77-2

Formula: C₁₆H₁₂O

Purity: 98%

Molecular weight: 220.2659

Ref: IN-DA00296B

1-(Phenanthren-9-yl)ethan-1-one

CAS: 2039-77-2

1-(Phenanthren-9-yl)ethan-1-one

Purity: 98%

Molecular weight: 220.27g/mol

Ref: 54-OR93065

1-(Phenanthren-9-yl)ethan-1-one

CAS: 2039-77-2

Color and Shape: Solid

Molecular weight: 220.271

Ref: 10-F982764

9-Acetylphenanthrene

CAS: 2039-77-2

9-Acetylphenanthrene is a pyridinium salt with triazolium and reduction products. The reduction products are formed by the reaction of the 9-acetylphenanthrene with chlorine atom or activated cyclic hydrocarbons. 9-Acetylphenanthrene has been shown to have glucocorticoid receptor affinity, which is due to its ability to bind to the hormone receptor in the cell membrane. This binding inhibits the interaction of cortisol with this receptor, preventing the activation of transcriptional responses that regulate gene expression. 9-Acetylphenanthrene also relaxes smooth muscle cells, which may be due to inhibition of calcium ion release from intracellular stores in response to acetylcholine.

Formula: C₁₆H₁₂O

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 220.27 g/mol

Ref: 3D-FA67349