The chemical substance known as (1R,4S)-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptane-1-carboxylate, with the CAS number 6703-31-7, is a bicyclic compound characterized by its unique structural features. It contains a bicyclo[2.2.1]heptane framework, which is a saturated bicyclic system, and features a carboxylate functional group that contributes to its reactivity and solubility in various solvents. The presence of multiple methyl groups at specific positions on the bicyclic structure enhances its steric bulk and can influence its physical properties, such as boiling and melting points. The ketone functional group (3-oxo) indicates that it has potential for further chemical reactivity, particularly in condensation reactions or as a precursor in synthetic pathways. This compound may exhibit interesting biological activities due to its structural complexity, making it a subject of interest in organic synthesis and medicinal chemistry. Its stereochemistry, denoted by the (1R,4S) configuration, suggests specific spatial arrangements that can affect its interactions with biological targets.

(1R,4S)-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptane-1-carboxylate

6703-31-7: The chemical substance known as (1R,4S)-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptane-1-carboxylate, with the CAS number 6703-31-7, is a bicyclic compound characterized by its unique structural features. It contains a bicyclo[2.2.1]heptane framework, which is a saturated bicyclic system, and features a carboxylate functional group that contributes to its reactivity and solubility in various solvents. The presence of multiple methyl groups at specific positions on the bicyclic structure enhances its steric bulk and can influence its physical properties, such as boiling and melting points. The ketone functional group (3-oxo) indicates that it has potential for further chemical reactivity, particularly in condensation reactions or as a precursor in synthetic pathways. This compound may exhibit interesting biological activities due to its structural complexity, making it a subject of interest in organic synthesis and medicinal chemistry. Its stereochemistry, denoted by the (1R,4S) configuration, suggests specific spatial arrangements that can affect its interactions with biological targets.

CAS 6703-31-7

(1R,4S)-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptane-1-carboxylate

4,7,7-Trimethyl-3-oxobicyclo[2.2.1]heptane-1-carboxylic Acid

Ref: TR-B537008