PI11347 (S)-(+)-2-Chlorophenylglycine methyl ester (CAS No.: 141109-14-0)

(S)-(+)-2-Chlorophenylglycine methyl ester (CAS No.: 141109-14-0) Description

(S)-(+)-2-Chlorophenylglycine methyl ester, with the molecular formula C9H10ClNO2 and CAS Number 141109-14-0, serves as an important building block in pharmaceutical synthesis. Its defined stereochemistry facilitates controlled chiral interactions during chemical reactions, contributing to consistent enantiomeric outcomes. Manufactured under strict quality protocols, this amino acid derivative is utilised in complex synthetic sequences to achieve the desired molecular configurations in active pharmaceutical ingredients.

(S)-(+)-2-Chlorophenylglycine methyl ester (CAS No.: 141109-14-0) Applications

1.       Pharmaceutical Manufacturing
- Used as a chiral building block in drug synthesis to improve reaction specificity by leveraging its defined enantiomeric purity.
- Applied in process development to optimise synthetic routes in producing active pharmaceutical ingredients.

2.       Research and Development
- Employed in experimental setups for studying stereochemical reaction mechanisms, enhancing understanding of enantioselective processes.
- Serves as a model compound in developing new methods for chiral resolution, directly impacting synthesis efficiency.

(S)-(+)-2-Chlorophenylglycine methyl ester (CAS No.: 141109-14-0) Packing

The compound is packaged in sealed, inert, moisture-proof containers lined with anti-static material. It is stored under controlled temperature and humidity conditions to minimise contamination and degradation. The packaging design includes secondary protective layers to prevent mechanical stress. Customers can opt for additional customisation such as vacuum sealing and nitrogen purging for enhanced protection and traceability.

Additional Information

Chiral pharmaceutical intermediates are vital in the production of enantiomerically pure drugs, as their inherent stereochemistry influences biological activity. Utilising advanced analytical techniques such as chiral chromatography alongside HPLC and NMR ensures these compounds meet stringent quality demands. Researchers continually study these intermediates to improve synthetic efficiency and optimise reaction conditions.

Amino acid derivatives like (S)-(+)-2-Chlorophenylglycine methyl ester contribute significantly to the development of complex molecules. Their controlled chirality aids in the refinement of reaction pathways, ultimately enhancing the predictability and reproducibility of pharmaceutical manufacturing processes.