(S)-3-Amino-1-carbobenzoxypyrrolidine Hydrochloride TCI A2324

Chemical Identity

CAS No.: 550378-39-7
PubChem: CID 20820180·SID 125307421
Formula: C12H17ClN2O2
Molecular weight: 256.73 g/mol
Purity: >98.0%(HPLC)(N)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: benzyl (3S)-3-aminopyrrolidine-1-carboxylate;hydrochloride
SMILES: C1CN(C[C@H]1N)C(=O)OCC2=CC=CC=C2.Cl
InChIKey: QNQVBYGRFHOBNO-MERQFXBCSA-N

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(S)-3-Amino-1-carbobenzoxypyrrolidine Hydrochloride is a chiral compound widely used in asymmetric synthesis to construct molecules with optical activity. This material plays a crucial role in chemical laboratories, especially those focused on chiral synthesis. Its unique structure allows it to serve as a building block for creating complex organic molecules with specific stereochemistry. As a key component in chiral synthesis, it enables researchers to achieve precise control over the spatial arrangement of atoms in a molecule, which is essential for developing compounds with desired biological activity.

The compound's properties make it a preferred choice for synthetic chemists. Its carbobenzoxy (Cbz) group provides stability and enhances reactivity, making it easier to modify during chemical reactions. Additionally, its solubility in organic solvents facilitates purification and reaction processes. The chiral nature of this compound ensures that only the desired enantiomer is produced, which is critical in pharmaceutical and biochemical applications. These characteristics make it an essential tool for researchers aiming to achieve high stereochemical control in their experiments.

In Indonesian laboratories, this compound is commonly used in pharmaceutical research, organic synthesis, and biochemistry. It is particularly valuable in drug development, where the stereochemistry of a molecule can significantly affect its biological activity. Its application extends to academic and industrial research settings, where precision in chemical synthesis is paramount. Researchers rely on this compound to produce chiral molecules with specific functions, contributing to advancements in medicinal chemistry and related fields.

TCI brochures (PDF)

Chiral Building Blocks 2025-04-14 · p. 3

Related TCI products

Asymmetric synthesis is a key application where this compound is used to create chiral molecules with specific stereochemistry, ensuring the production of the desired enantiomer for pharmaceutical and biochemical applications.
Organic synthesis relies on this compound as a chiral building block, enabling the construction of complex molecules with precise stereochemical control, which is essential for drug development and chemical research.
Pharmaceutical research benefits from this compound's ability to produce chiral compounds with specific biological activity, making it valuable in the development of new drugs and therapeutic agents.
Biochemical studies utilize this compound to investigate the effects of stereochemistry on molecular interactions, aiding in the understanding of enzyme mechanisms and receptor binding.
Academic research in chemistry and pharmacology employs this compound to explore new synthetic pathways and to develop compounds with enhanced pharmacological properties.

Brand	TCI
CAS number	550378-39-7
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from light

This compound should be stored in a cool, dry place, away from direct light to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Proper labeling of containers is essential for safe handling and identification. Due to its chiral nature, it is important to maintain strict handling protocols to avoid cross-contamination. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in chemical synthesis and research applications.

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