N-(tert-Butoxycarbonyl)-D-prolinol TCI B3076

Chemical Identity

CAS No.: 83435-58-9
PubChem: CID 688279·SID 87559821
Formula: C10H19NO3
Molecular weight: 201.26 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tert-butyl (2R)-2-(hydroxymethyl)pyrrolidine-1-carboxylate
SMILES: CC(C)(C)OC(=O)N1CCC[C@@H]1CO
InChIKey: BFFLLBPMZCIGRM-MRVPVSSYSA-N

Rp 610.050,00

~~Rp 442.050,00~~ Rp 610.050,00

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N-(tert-Butoxycarbonyl)-D-prolinol is a chiral building block widely used in asymmetric synthesis to construct molecules with optical activity. This compound plays a crucial role in laboratory settings where precise control over molecular structure and optical properties is essential. It is commonly employed in the development of pharmaceuticals, organic chemicals, and bioactive compounds. Its ability to participate in chiral-controlled reactions makes it an indispensable tool for chemists working on complex molecular architectures.

The compound’s chiral nature and stability under specific reaction conditions make it a preferred choice for synthetic chemists. Its ability to maintain stereochemical integrity during reactions ensures reliable outcomes in asymmetric synthesis. This characteristic is especially valuable in the production of enantiomerically pure compounds, which are critical in pharmaceutical applications. The compound’s chemical stability further enhances its utility, allowing for consistent performance across various experimental protocols.

In Indonesian laboratories, N-(tert-Butoxycarbonyl)-D-prolinol is frequently used in organic chemistry research, particularly in pharmaceutical and bioactive compound synthesis. Local researchers rely on this compound for developing new products that require precise molecular control. Its role in creating optically active molecules is vital for advancing drug discovery and chemical innovation in the region.

TCI brochures (PDF)

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

Related TCI products

Asymmetric synthesis of optically active pharmaceutical compounds due to its chiral structure and controlled reactivity.
Development of bioactive molecules requiring precise stereochemical control for enhanced biological activity.
Organic chemistry research focused on chiral building blocks for complex molecule construction.
Pharmaceutical compound synthesis where enantiomeric purity is essential for drug efficacy and safety.
Advanced chemical synthesis projects involving chiral intermediates for industrial and academic applications.

Brand	TCI
CAS number	83435-58-9
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid (exact form may vary based on supplier packaging)
Storage	Store in a cool, dry place away from moisture and direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent moisture absorption, which could compromise its integrity. For optimal preservation, it should be stored away from direct sunlight and sources of heat. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. Proper labeling of storage containers is essential for safe handling and to prevent accidental exposure. Regular monitoring of storage conditions ensures the compound remains suitable for use in chemical synthesis processes.

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