CAS 362-46-9

Methanone, (2-amino-5-fluorophenyl)phenyl-

Description:

Methanone, (2-amino-5-fluorophenyl)phenyl- is an organic compound characterized by its structure, which includes a methanone functional group attached to a phenyl ring that is further substituted with an amino group and a fluorine atom. This compound is part of the class of ketones and is known for its potential applications in pharmaceuticals and agrochemicals due to its unique chemical properties. The presence of the amino group contributes to its basicity and potential reactivity in various chemical reactions, while the fluorine atom can enhance lipophilicity and influence biological activity. Methanone derivatives often exhibit interesting pharmacological properties, making them subjects of research in medicinal chemistry. The compound's molecular structure allows for various interactions, including hydrogen bonding and π-π stacking, which can affect its solubility and stability. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

Formula: C₁₃H₁₀FNO

Synonyms:

• (2-Amino-5-fluorophenyl)(phenyl)methanone

5-fluoro-2-aMinobenzophenone

CAS: 362-46-9

Formula: C₁₃H₁₀FNO

Purity: %

Color and Shape: Solid

Molecular weight: 215.2230

Ref: IN-DA00CLLD

(2-Amino-5-fluorophenyl)(phenyl)methanone

CAS: 362-46-9

(2-Amino-5-fluorophenyl)(phenyl)methanone

Purity: 95%

Molecular weight: 215.22g/mol

Ref: 54-PC907525

2-AMINO-5-FLUOROBENZOPHENONE

CAS: 362-46-9

Formula: C₁₃H₁₀FNO

Purity: 95+%

Molecular weight: 215.227

Ref: 10-F470704

(2-Amino-5-fluorophenyl)(phenyl)methanone

CAS: 362-46-9

2-Amino-5-fluorophenyl)(phenyl)methanone is a hydrogen bond acceptor that binds to the benzodiazepine receptor. Hydrogen bonds are formed by dipole interactions between the hydrogen atom of a donor molecule and the electronegative atoms of a receptor. This interaction is characterized by a high affinity, which makes it useful for medicinal chemistry. 2-Amino-5-fluorophenyl)(phenyl)methanone has been shown to interact with brain membranes and has been used in medicine as an anxiolytic agent. It produces its effects by enhancing the activity of GABA, an inhibitory neurotransmitter, at the benzodiazepine receptor site on GABA receptors in the brain. The drug also has some affinity for binding to other sites in the central nervous system, such as at GABA receptors in cortical neurons, pyramidal cells in hippocampus, and ventral tegmental area dopamine neurons.

Formula: C₁₃H₁₀FNO

Purity: Min. 95%

Molecular weight: 215.23 g/mol

Ref: 3D-AAA36246