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Product Line: Pharmaceutical Chemicals

2,2,2-Trichloroethyl chloroformate

CAS 17341-93-4

Molecular structure of 2,2,2-Trichloroethyl chloroformate

CAS · 17341-93-4

01

Product Overview

2,2,2-Trichloroethyl chloroformate is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance: Colorless liquid
Assay (GC): 98.5% min.
03

Applications

 

 

1. Organic Synthesis Intermediate

Used primarily as a protecting group reagent in organic synthesis.

Protects amino groups as carbamates via reaction with amines, enabling selective reactions on multifunctional molecules.

The 2,2,2-trichloroethyl group can be cleaved reductively, allowing temporary protection.

2. Pharmaceutical Synthesis

Applied in the synthesis of pharmaceutical intermediates where protection/deprotection strategies are critical.

Facilitates the synthesis of complex molecules by preventing side reactions on amine functionalities.

3. Peptide Chemistry

Utilized to protect amino groups during peptide synthesis, allowing stepwise construction of peptides without undesired side reactions.

4. Polymer and Material Chemistry

Employed in the synthesis of functionalized polymers and monomers where carbamate groups impart desirable properties.

04

Benefits

Effective Protecting Group: Provides robust protection for amines under diverse reaction conditions.

Selective and Reversible: The 2,2,2-trichloroethyl group can be removed under mild reductive conditions, making it a practical choice.

Improves Synthetic Efficiency: Enables multi-step synthesis by preventing unwanted reactions.

Compatibility: Compatible with various organic solvents and reagents.

05

Conclusion

2,2,2-Trichloroethyl chloroformate (CAS 17341-93-4) is a specialized reagent used mainly as a protecting group agent in organic and pharmaceutical synthesis. Its ability to selectively protect amino groups and be cleaved under mild conditions makes it invaluable for complex multi-step syntheses, including peptide production. Despite its reactivity, it enables improved efficiency and selectivity when handled with appropriate safety measures.

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