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Home  > (2S,5R)-6-(Benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acid

AA18255

1174020-25-7 | (2S,5R)-6-(Benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $25.00 $18.00 -   +
250mg 97% in stock $28.00 $20.00 -   +
1g 97% in stock $58.00 $41.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA18255
Chemical Name: (2S,5R)-6-(Benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acid
CAS Number: 1174020-25-7
Molecular Formula: C14H16N2O4
Molecular Weight: 276.2878
MDL Number: MFCD28502389
SMILES: OC(=O)[C@@H]1CC[C@@H]2CN1C(=O)N2OCc1ccccc1

 

Upstream Synthesis Route
  • The compound (2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acid, hereinafter referred to as "$name$," serves as a versatile building block in chemical synthesis. Known for its unique structural features, $name$ plays a crucial role as a precursor in the preparation of various bioactive molecules and pharmaceutical intermediates.In chemical synthesis, $name$ is commonly utilized as a key component in the construction of complex organic compounds due to its functional groups and stereochemical arrangement. Its diazabicyclo[3.2.1]octane core provides a rigid and stable framework for selective reactions, making it a valuable starting material for producing intricate molecular structures.One of the prominent applications of $name$ in chemical synthesis is its role as a chiral scaffold for asymmetric synthesis. With its defined stereochemistry at the 2S and 5R positions, $name$ allows for the controlled formation of chiral centers, enabling the synthesis of enantiomerically pure compounds essential in pharmaceutical development and agrochemical research.Moreover, the presence of the carboxylic acid group in $name$ offers functionalization potential, enabling further derivatization through esterification, amidation, or other chemical transformations. This flexibility in modification enhances the versatility of $name$ in custom synthesis pathways tailored to specific target molecules.Overall, (2S,5R)-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carboxylic acid, or $name$, stands out as a pivotal molecule in the realm of chemical synthesis, facilitating the creation of complex structures with defined stereochemistry and functional diversity.
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