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TCI

CAS 102089-74-7

N-(tert-Butoxycarbonyl)-D-2-phenylglycinol TCI B3270

N-(tert-Butoxycarbonyl)-D-2-phenylglycinol TCI B3270

Chemical Identity

CAS No.
102089-74-7
PubChem
CID 7016461·SID 87560975
Formula
C13H19NO3
Molecular weight
237.29 g/mol
Purity
>97.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl N-[(1R)-2-hydroxy-1-phenylethyl]carbamate
SMILES
CC(C)(C)OC(=O)N[C@@H](CO)C1=CC=CC=C1
InChIKey
IBDIOGYTZBKRGI-NSHDSACASA-N
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N-(tert-Butoxycarbonyl)-D-2-phenylglycinol is a chiral building block widely used in asymmetric synthesis, playing a crucial role in the development of chiral compounds. This compound is essential for creating molecules with specific spatial configurations, which is vital in pharmaceutical and organic chemistry research. Its unique structure allows for precise control over the stereochemistry of the final product, making it a key component in the synthesis of bioactive molecules. Due to its stability and reactivity, it is frequently employed in advanced chemical processes requiring high selectivity.

The compound’s chiral nature and the presence of the tert-butoxycarbonyl group make it a preferred choice for synthetic chemists. The tert-butoxycarbonyl group provides structural stability while allowing for controlled chemical transformations under specific reaction conditions. This makes it highly versatile in a variety of synthetic pathways. Its ability to act as a chiral auxiliary is particularly valuable in the preparation of enantiomerically pure compounds, which are essential in drug development and other specialized chemical applications.

In Indonesian laboratories, N-(tert-Butoxycarbonyl)-D-2-phenylglycinol is commonly used in organic chemistry research, especially in asymmetric synthesis and pharmaceutical development. It is a staple in academic and research institutions where precision and control over molecular structure are paramount. Its solid form facilitates easy handling and storage, making it a practical choice for laboratory use.

TCI brochures (PDF)

  • Asymmetric synthesis is a key application where this compound serves as a chiral auxiliary, enabling the selective formation of enantiomers with high stereocontrol.
  • Organic chemistry research benefits from its structural stability and reactivity, allowing for the synthesis of complex molecules with specific stereochemistry.
  • Pharmaceutical development relies on its ability to produce chiral compounds with desired biological activity, supporting drug discovery and formulation.
  • Chiral building block applications are widespread in synthetic chemistry, where precise control over molecular structure is required for advanced chemical processes.
  • Academic and research institutions use it for high-precision experiments, particularly in the study of stereochemistry and molecular interactions.

Brand TCI
CAS number 102089-74-7
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent contamination and maintain its chemical integrity. Due to its chiral nature, it is important to handle it with care to avoid any unintended stereochemical changes. Proper labeling and storage conditions are essential to ensure its effectiveness in laboratory applications. Always follow standard chemical safety protocols when handling and using this compound in a laboratory setting.

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