PI11322 rac-Des(4-cyclohexyl-L-proline) Fosinopril Acetic Acid (CAS No.: 123599-78-0)

[(2-Methyl-1-propionylpropoxy)(4-phenylbutyl)phosphinoyl]acetic acid (CAS No.: 123599-78-0) Description

[(2-Methyl-1-propionylpropoxy)(4-phenylbutyl)phosphinoyl]acetic acid, with a molecular formula of C19H29O6P and a CAS registry number of 123599-78-0, is provided as a fine powder for pharmaceutical synthesis. Its controlled reactivity and purity are confirmed through rigorous analytical methods. The compound's defined chemical structure supports its use as an intermediate in complex synthetic routes, aiding the construction of advanced molecular entities.

[(2-Methyl-1-propionylpropoxy)(4-phenylbutyl)phosphinoyl]acetic acid (CAS No.: 123599-78-0) Applications

1.         Pharmaceutical Synthesis
   - Used as an intermediate in API development to achieve targeted molecular assembly by leveraging its defined reactivity profile.
   - Applied as a reagent in multi-step syntheses to facilitate the construction of complex active molecules with consistent performance.

2.         Chemical Manufacturing
   - Serves as a building block in the production of speciality chemicals, enabling the introduction of specific functional groups and maintaining batch-to-batch reproducibility.

[(2-Methyl-1-propionylpropoxy)(4-phenylbutyl)phosphinoyl]acetic acid (CAS No.: 123599-78-0) Packing

The product is packaged in moisture-resistant, sealed containers with inert, anti-static lining to prevent exposure to environmental humidity. These containers are designed to minimise particulate contamination while ensuring chemical stability. The packaging supports proper storage in cool, dry conditions and meets handling requirements for sensitive pharmaceutical intermediates. Custom options are available for specialised transportation or storage needs.

Additional Information

Chemical intermediates such as this compound play a crucial role in the synthesis of complex pharmaceutical molecules. Understanding the controlled reactivity and precise molecular composition is essential for integrating such materials into multi-step synthetic processes. Detailed knowledge of the compound's behaviour under various conditions supports improvements in yield and process efficiency.

Advances in analytical methods continue to refine quality control in chemical synthesis. By employing techniques such as HPLC, NMR, and mass spectrometry, manufacturers can verify the integrity of intermediates, ensuring that each batch meets the rigorous standards required in pharmaceutical production.