N-(tert-Butoxycarbonyl)-L-2-phenylglycinol is a chiral building block widely used in asymmetric synthesis within laboratory settings. This compound plays a crucial role in the development of complex molecules with specific stereochemical configurations, which are essential in pharmaceutical and materials science research. Its utility lies in its ability to serve as a versatile intermediate in the synthesis of optically active compounds, offering researchers precise control over molecular structure. In Indonesian laboratories, this compound is a key component in the study of chiral molecules, supporting advancements in drug discovery and chemical innovation.
The compound’s stability and reactivity make it a preferred choice for synthetic chemists. The presence of the tert-butoxycarbonyl (Boc) group enhances its resistance to premature degradation, allowing it to remain chemically stable during various reaction conditions. This feature is particularly beneficial in multi-step syntheses where maintaining the integrity of the chiral center is critical. Additionally, its compatibility with a range of chemical reactions, including hydrolysis and substitution, makes it adaptable to diverse synthetic strategies. These properties ensure its effectiveness in both academic and industrial research environments.
In Indonesian laboratories, N-(tert-Butoxycarbonyl)-L-2-phenylglycinol is commonly used in organic chemistry research, especially in asymmetric synthesis and chiral compound development. Its role is vital in the creation of biologically active molecules, supporting the work of researchers in both academic and applied settings. The compound’s reliability and performance make it a standard choice for those requiring precision in their chemical processes.
TCI brochures (PDF)
- Chiral Building Blocks 2025-04-14 · p. 7
Related TCI products
- TCI B3270 102089-74-7 N-(tert-Butoxycarbonyl)-D-2-phenylglycinol
- TCI B2604 66605-57-0 N-(tert-Butoxycarbonyl)-L-phenylalaninol
- TCI B1966 106454-69-7 N-(tert-Butoxycarbonyl)-D-phenylalaninol
- TCI B3230 33125-05-2 N-(tert-Butoxycarbonyl)-D-2-phenylglycine
- TCI B3211 2900-27-8 N-(tert-Butoxycarbonyl)-L-2-phenylglycine
- TCI F1193 111524-95-9 N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-2-phenylglycine
- Asymmetric synthesis is a key application where this compound is used to create chiral molecules with specific stereochemistry, essential for drug development and pharmaceutical research.
- Chiral compound development benefits from its ability to serve as a building block, allowing researchers to design and synthesize complex molecules with desired optical properties.
- Organic chemistry research utilizes this compound in the synthesis of various functional groups, supporting the exploration of new chemical structures and reactivity patterns.
- Pharmaceutical research leverages its role in the creation of biologically active compounds, contributing to the development of new therapeutic agents.
- Material science applications benefit from its use in the synthesis of specialized polymers and other advanced materials with controlled stereochemistry.
| Brand | TCI |
|---|---|
| CAS number | 117049-14-6 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Asymmetric Synthesis > Chiral Building Blocks |
| Pack sizes | Available in various quantities as per supplier listings |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from light and moisture |
This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and air, which may affect its stability. Proper labeling of containers is essential for safe handling and to avoid cross-contamination. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during synthesis and experimentation. Regular monitoring of storage conditions is advised to ensure optimal performance and longevity of the compound.
—
Product Categories
- Asymmetric SynthesisChiral Building BlocksChiral Non-Heterocyclic Building Blocks
- Building BlocksChiral Building BlocksChiral Non-Heterocyclic Building Blocks
- Chemical BiologyPeptide ChemistryAmino Acid Derivatives [Peptide Chemistry]
- Pharmaceutical Development and Drug Discovery Research ReagentsPeptide ChemistryAmino Acid Derivatives [Peptide Chemistry]





![N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-D-2-phenylglycine (CAS 111524-95-9) - TCI F1193 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510F1193.jpg?v=1768205447&width=533)
![N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-2-phenylglycine (CAS 102410-65-1) - TCI F0669 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510F0669.jpg?v=1771058185&width=533)
