CAS 25023-01-2

9,9-Dichlorofluorene

Description:

9,9-Dichlorofluorene is an organic compound characterized by its structure, which features a fluorene backbone with two chlorine substituents at the 9-position. This compound is typically a solid at room temperature and is known for its aromatic properties, which contribute to its stability and potential applications in organic synthesis and materials science. The presence of chlorine atoms introduces unique reactivity and polarity, making it useful in various chemical reactions, including electrophilic substitution. 9,9-Dichlorofluorene may exhibit moderate solubility in organic solvents, while its physical properties, such as melting and boiling points, can be influenced by the presence of the chlorine substituents. Safety considerations are important when handling this compound, as halogenated compounds can pose environmental and health risks. Overall, 9,9-Dichlorofluorene serves as an interesting subject for research in organic chemistry and materials development due to its distinctive structural features and reactivity.

Formula: C₁₃H₈Cl₂

InChI: InChI=1S/C13H8Cl2/c14-13(15)11-7-3-1-5-9(11)10-6-2-4-8-12(10)13/h1-8H

InChI key: InChIKey=LSTBDYVWQHHYHU-UHFFFAOYSA-N

SMILES: ClC1(Cl)C=2C(C=3C1=CC=CC3)=CC=CC2

Synonyms:

• 9,9-Dichlorlo-9H-fluorene
• 9,9-Dichlorofluorene
• 9H-Fluorene, 9,9-dichloro-
• Fluorene, 9,9-dichloro-
• NSC 111101
• 9,9-Dichloro-9H-fluorene

9,9-Dichloro-9H-fluorene

CAS: 25023-01-2

Formula: C₁₃H₈Cl₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 235.1086

Ref: IN-DA003NJQ

9,9-Dichloro-9H-fluorene

CAS: 25023-01-2

Purity: 95.0%

Color and Shape: Solid

Molecular weight: 235.11000061035156

Ref: 10-F211567

9,9-Dichlorofluorene

CAS: 25023-01-2

9,9-Dichlorofluorene is a bifluorenylidene that reacts with hydrochloric acid to form the trifluoroacetate anion. It is nucleophilic and can be used in organic synthesis to form carbon-fluorine bonds or chloroformates. 9,9-Dichlorofluorene also reacts with chloride ions to form the chloride anion. This reaction yields a high yield and has been used to synthesize other chemicals, including thioacetals and dimethylformamide. 9,9-Dichlorofluorene reacts with protonated nucleophiles in DMF and forms thioacetals following deprotection by hydrochloric acid. The reaction yield of this process is high and it has been extensively studied by NMR spectroscopy.

Formula: C₁₃H₈Cl₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 235.11 g/mol

Ref: 3D-FD147233