CAS 3403-70-1

1,1'-(9H-carbazole-3,6-diyl)diethanone

Description:

1,1'-(9H-carbazole-3,6-diyl)diethanone, with the CAS number 3403-70-1, is an organic compound characterized by its structure, which features a carbazole moiety linked to two ethyl ketone groups. This compound exhibits properties typical of both aromatic and ketone functionalities, contributing to its potential applications in organic electronics and materials science. The presence of the carbazole unit imparts notable photophysical properties, making it a candidate for use in light-emitting devices and organic semiconductors. Additionally, the compound may exhibit fluorescence, which can be influenced by its molecular environment and substituents. Its solubility in organic solvents is expected, facilitating its use in various chemical reactions and applications. The compound's reactivity is primarily governed by the ketone groups, which can participate in nucleophilic addition reactions. Overall, 1,1'-(9H-carbazole-3,6-diyl)diethanone is a versatile compound with potential utility in advanced materials and organic synthesis.

Formula: C₁₆H₁₃NO₂

InChI: InChI=1/C16H13NO2/c1-9(18)11-3-5-15-13(7-11)14-8-12(10(2)19)4-6-16(14)17-15/h3-8,17H,1-2H3

Synonyms:

• 1,1'-(9H-Carbazole-3,6-diyl)diethanone
• 1-(6-Acetyl-9H-carbazol-3-yl)-ethanone
• Ethanone, 1,1'-(9H-carbazole-3,6-diyl)bis-

1,1'-(9H-Carbazole-3,6-diyl)diethanone

CAS: 3403-70-1

Formula: C₁₆H₁₃NO₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 251.2799

Ref: IN-DA00CKDU

1,1'-(9H-Carbazole-3,6-diyl)bis(ethan-1-one)

CAS: 3403-70-1

1,1'-(9H-Carbazole-3,6-diyl)bis(ethan-1-one)

Purity: 97%

Molecular weight: 251.28g/mol

Ref: 54-OR86427

1,1-(9H-carbazole-3,6-diyl)diethanone

CAS: 3403-70-1

1,1-(9H-carbazole-3,6-diyl)diethanone is an aromatic compound with a molecular formula of C12H10N2O that belongs to the class of enol ethers. It can be used as a framework for the synthesis of other compounds. The acylation reaction is catalyzed by a transfer catalyst and carried out in dioxane at room temperature. After filtration and washing with deionized water, it is then dried under vacuum to yield the product. Friedel-Crafts acylation or a metal salt may be used during this process. 1,1-(9H-carbazole-3,6-diyl)diethanone has also been shown to act as a ligand for transition metals such as copper and zinc in certain reactions.

Formula: C₁₆H₁₃NO₂

Purity: Min. 95%

Molecular weight: 251.28 g/mol

Ref: 3D-DAA40370