CAS 345-69-7

3-Fluorobenzophenone

Description:

3-Fluorobenzophenone, with the CAS number 345-69-7, is an organic compound characterized by the presence of a fluorine atom attached to a benzophenone structure. It features a central carbonyl group (C=O) flanked by two phenyl rings, one of which has a fluorine substituent in the meta position relative to the carbonyl. This compound is typically a white to light yellow solid at room temperature and is known for its role in organic synthesis and as a photoinitiator in polymer chemistry. Its molecular formula is C13H9FO, and it exhibits properties such as moderate solubility in organic solvents. The presence of the fluorine atom can influence its reactivity and physical properties, including its electronic characteristics and potential applications in materials science. Additionally, 3-fluorobenzophenone may be used in the development of UV filters and in the synthesis of various pharmaceuticals and agrochemicals, making it a compound of interest in both industrial and research settings.

Formula: C₁₃H₉FO

Synonyms:

• 3-Fluorobenzophenone,98%
• 3-fluorobenzephenone
• 3-Fluorobenzophenone 98%
• 3-FLUOROBENZOPHENONE
• (3-Fluorophenyl)(phenyl)methanone
• Methanone, (3-fluorophenyl)phenyl-

3-Fluorobenzophenone

CAS: 345-69-7

Formula: C₁₃H₉FO

Purity: 98%

Color and Shape: Solid

Molecular weight: 200.2084

Ref: IN-DA00C123

3-Fluorobenzophenone

CAS: 345-69-7

3-Fluorobenzophenone

Formula: C₁₃H₉FO

Purity: 98%

Color and Shape: colorless solid

Molecular weight: 200.21g/mol

Ref: 54-PC9753

3-Fluorobenzophenone

CAS: 345-69-7

Formula: C₁₃H₉FO

Purity: 97%

Color and Shape: Clear

Molecular weight: 200.212

Ref: 10-F024623

3-Fluorobenzophenone

CAS: 345-69-7

3-Fluorobenzophenone is a functionalized organic compound that can be synthesized by the reaction of potassium t-butoxide with 3-fluorobenzaldehyde. This chemical has been shown to have vibrational bands in the infrared region of the electromagnetic spectrum. The protonation and acidic properties of 3-fluorobenzophenone were confirmed by control experiments involving hydrogenation reactions with carboxylic acids and nucleophilic acetonitrile, respectively.
3-Fluorobenzophenone is soluble in water and alcohols, but insoluble in ethers; it is stable under normal conditions, but decomposes when heated or exposed to UV light.

Formula: C₁₃H₉FO

Purity: Min. 95%

Molecular weight: 200.21 g/mol

Ref: 3D-FF67608