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CAS 82689-19-8

Nalpha-(tert-Butoxycarbonyl)-L-tryptophanol TCI B4287

Nalpha-(tert-Butoxycarbonyl)-L-tryptophanol TCI B4287

Chemical Identity

CAS No.
82689-19-8
PubChem
CID 7019533·SID 253661480
Formula
C16H22N2O3
Molecular weight
290.36 g/mol
Purity
>98.0%(HPLC)(N)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
tert-butyl N-[(2S)-1-hydroxy-3-(1H-indol-3-yl)propan-2-yl]carbamate
SMILES
CC(C)(C)OC(=O)N[C@@H](CC1=CNC2=CC=CC=C21)CO
InChIKey
JEFQUFUAEKORKL-LBPRGKRZSA-N
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TCI B4287 Nalpha-(tert-Butoxycarbonyl)-L-tryptophanol is a chiral building block essential in asymmetric synthesis, particularly for the preparation of chiral compounds. This compound plays a crucial role in laboratories where precise control over stereochemistry is required. Its unique molecular structure enables chemists to design and synthesize complex molecules with specific spatial configurations. It is widely used in both academic and industrial research settings to develop new pharmaceuticals and organic chemicals.

The compound's stability and reactivity make it a preferred choice in synthetic chemistry. The tert-butoxycarbonyl group provides structural stability, allowing for controlled chemical transformations. This feature is vital in achieving high yields and purity in asymmetric reactions. Additionally, its compatibility with various reaction conditions ensures versatility in experimental setups. These properties make it a reliable tool for researchers aiming to produce chiral compounds with high specificity.

In Indonesian laboratories, this compound is commonly used by researchers in educational institutions and research organizations. It supports the development of new drugs and bioactive compounds, especially in pharmacology and medicinal chemistry. Its availability in different packaging options allows for flexible use across various experimental scales. The compound’s role in stereoselective synthesis makes it a key component in advanced chemical research in Indonesia.

TCI brochures (PDF)

  • Asymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the creation of enantiomerically pure compounds.
  • Pharmaceutical Development: It supports the synthesis of chiral pharmaceuticals, which are essential for drug development with specific biological activity.
  • Organic Chemistry Research: Its reactivity and stability make it a valuable reagent in organic synthesis, especially in complex molecule construction.
  • Medicinal Chemistry Studies: It is widely used in medicinal chemistry for the design of bioactive compounds with precise stereochemical configurations.
  • Academic Research: It is a key material in academic laboratories for teaching and research in synthetic chemistry and stereochemistry.

Brand TCI
CAS number 82689-19-8
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in multiple packaging options for different experimental needs
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Proper labeling of storage containers is essential for safe handling and identification. In a laboratory setting, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible materials and ensure proper ventilation when working with this compound. Regular monitoring of storage conditions helps in maintaining the quality and effectiveness of the material for research purposes.

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