N-(tert-Butoxycarbonylamino)phthalimide: A Versatile Reagent for Organic Synthesis and Research Applications

Unlock new possibilities in your chemical synthesis with this essential building block.

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Key Advantages

Versatile Reactivity

This compound serves as a crucial reagent in the Mitsunobu reaction, enabling the transformation of alcohols into valuable intermediates, a core aspect of exploring organic synthesis building block applications.

Protected Amino Functionality

The tert-butoxycarbonyl (Boc) protecting group offers strategic advantages in multistep syntheses, allowing for controlled reactions and selective deprotection when needed, which is key for precise organic synthesis.

High Purity and Reliability

Ensuring consistent quality is paramount for research success. This reagent is supplied with high purity, critical for achieving accurate results in complex reaction schemes and CAS 34387-89-8 applications.

Key Applications

Alcohol to Carbazate/Hydrazine Conversion

Utilize N-(tert-Butoxycarbonylamino)phthalimide for the efficient conversion of alcohols, a foundational step in synthesizing various organic compounds.

Pharmaceutical Intermediate Synthesis

This reagent is indispensable in the development of pharmaceutical intermediates, supporting the creation of molecules with potential therapeutic benefits.

Research and Development

Its well-defined reactivity profile makes it a preferred choice for researchers exploring new synthetic methodologies and novel chemical entities.

Peptide Synthesis

As a protected amino compound, it finds application in specialized peptide synthesis protocols, contributing to the creation of complex biomolecules.