4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate(CAS: 9002-83-9)

4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate is a crystalline compound with a molecular weight of approximately 413.11 g/mol. It is moderately soluble in organic solvents like methanol and ethanol and slightly soluble in water. The compound is known for its reactivity towards nucleophiles, particularly due to the presence of carboxylic acid and hydroxyethyl functionalities.

4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate is synthesized through a multi-step process involving nitration of the benzyl group followed by a ring-opening reaction to introduce the azabicyclo[3.2.0]heptane structure. Common reactions include use of nitric acid, acetic anhydride, and other reagents. The product typically has a yield of 70-80%.

4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate is primarily used in the pharmaceutical industry for the development of drug molecules and in the polymer industry as a monomer. It also finds applications in sensor technology and semiconductor manufacturing due to its functional groups.

When handling 4-Nitrobenzyl (5R)-6-[(1R)-1-hydroxyethyl]-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate, it is important to wear appropriate personal protective equipment (PPE), including gloves, goggles, and a lab coat. Work should be conducted in a fume hood to minimize inhalation risks. Spills should be cleaned up using appropriate absorbents, and the material safety data sheet (MSDS) or safety data sheet (SDS) should be consulted for detailed instructions.