The chemical substance known as (2R,4S)-4-hydroxy-2-(3-methylbut-2-en-1-yl)-3,4-dihydronaphthalen-1(2H)-one, with the CAS number 34168-56-4, is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a naphthalene core, which is a polycyclic aromatic hydrocarbon, and includes a hydroxyl group (-OH) and a ketone group (C=O) that contribute to its reactivity and solubility properties. The presence of the 3-methylbut-2-en-1-yl substituent introduces additional steric and electronic effects, influencing its chemical behavior and potential biological activity. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its stereochemical configuration suggests that it may interact with biological targets in a specific manner, potentially leading to unique therapeutic effects. Overall, the compound's characteristics, including its molecular structure and functional groups, play a crucial role in determining its chemical reactivity and potential applications in various fields, including pharmaceuticals and organic synthesis.

(2R,4S)-4-hydroxy-2-(3-methylbut-2-en-1-yl)-3,4-dihydronaphthalen-1(2H)-one

34168-56-4: The chemical substance known as (2R,4S)-4-hydroxy-2-(3-methylbut-2-en-1-yl)-3,4-dihydronaphthalen-1(2H)-one, with the CAS number 34168-56-4, is a complex organic compound characterized by its specific stereochemistry and functional groups. It features a naphthalene core, which is a polycyclic aromatic hydrocarbon, and includes a hydroxyl group (-OH) and a ketone group (C=O) that contribute to its reactivity and solubility properties. The presence of the 3-methylbut-2-en-1-yl substituent introduces additional steric and electronic effects, influencing its chemical behavior and potential biological activity. This compound may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry. Its stereochemical configuration suggests that it may interact with biological targets in a specific manner, potentially leading to unique therapeutic effects. Overall, the compound's characteristics, including its molecular structure and functional groups, play a crucial role in determining its chemical reactivity and potential applications in various fields, including pharmaceuticals and organic synthesis.

1(2H)-Naphthalenone,3,4-dihydro-4-hydroxy- 2-(3-methyl-2-butenyl)-,(2R,4S)-

Catalponol

Catalponol boosts dopamine production and guards against L-DOPA toxicity in PC12 cells by raising cyclic AMP levels.

CAS 34168-56-4

(2R,4S)-4-hydroxy-2-(3-methylbut-2-en-1-yl)-3,4-dihydronaphthalen-1(2H)-one

1(2H)-Naphthalenone,3,4-dihydro-4-hydroxy- 2-(3-methyl-2-butenyl)-,(2R,4S)-

Ref: IN-DA007H88

Catalponol

Ref: BP-SBP01618

Catalponol

Ref: TM-TMA2419