The chemical substance known as "2H-1,4-Benzodiazepin-2-one, 3-amino-9-fluoro-1,3-dihydro-5-phenyl-, (3R)-" with CAS number 2436275-53-3 is a member of the benzodiazepine class, which is characterized by a fused benzene and diazepine ring structure. This compound features a fluorine atom at the 9-position and an amino group at the 3-position, contributing to its unique pharmacological properties. The presence of a phenyl group at the 5-position enhances its lipophilicity, potentially influencing its bioavailability and interaction with biological targets. The (3R)- designation indicates a specific stereochemistry, which can significantly affect the compound's activity and binding affinity to receptors. Benzodiazepines are known for their effects on the central nervous system, often exhibiting anxiolytic, sedative, and muscle relaxant properties. The specific characteristics of this compound, including its solubility, stability, and reactivity, would depend on its molecular structure and functional groups, making it a subject of interest for further pharmacological studies and potential therapeutic applications.

2H-1,4-Benzodiazepin-2-one, 3-amino-9-fluoro-1,3-dihydro-5-phenyl-, (3R)-

2436275-53-3: The chemical substance known as "2H-1,4-Benzodiazepin-2-one, 3-amino-9-fluoro-1,3-dihydro-5-phenyl-, (3R)-" with CAS number 2436275-53-3 is a member of the benzodiazepine class, which is characterized by a fused benzene and diazepine ring structure. This compound features a fluorine atom at the 9-position and an amino group at the 3-position, contributing to its unique pharmacological properties. The presence of a phenyl group at the 5-position enhances its lipophilicity, potentially influencing its bioavailability and interaction with biological targets. The (3R)- designation indicates a specific stereochemistry, which can significantly affect the compound's activity and binding affinity to receptors. Benzodiazepines are known for their effects on the central nervous system, often exhibiting anxiolytic, sedative, and muscle relaxant properties. The specific characteristics of this compound, including its solubility, stability, and reactivity, would depend on its molecular structure and functional groups, making it a subject of interest for further pharmacological studies and potential therapeutic applications.

(R)-3-amino-9-fluoro-5-phenyl-1H-benzo[e][1,4]diazepin-2(3H)-one

CAS 2436275-53-3

2H-1,4-Benzodiazepin-2-one, 3-amino-9-fluoro-1,3-dihydro-5-phenyl-, (3R)-

(R)-3-amino-9-fluoro-5-phenyl-1H-benzo[e][1,4]diazepin-2(3H)-one

Ref: 54-PC102851