Taiy Chemical
1-[(9H-Fluoren-9-ylmethoxy)carbonyl]proline
Product Name Fmoc-Pro-OH
Synonyms:103668 1,2-pyrrolidinedicarboxylic acid, 1-(9H-fluoren-9-ylmethyl) ester; 1-[(9H-Fluoren-9-ylmethoxy)carbonyl]proline; 1-[(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid; 1-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-proline; (2S)-1-[(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylate; Fmoc-L-Proline; Fmoc-L-Pro-OH
CAS RN. 71989-31-6
EINECS 276-259-0
Molecular Weight 336.3618
Molecular Formula C20H18NO4
Melting Point(℃) 112-115℃
Boiling Point(℃) 548.6°C at 760 mmHg
Flash Point(℃) 285.6°C
Hazard Symbols Xi Details
Xi
Risk Codes  R36/37/38;    Details
 R36/37/38;     Details
Safety Description  S26;S36;Details
 S26;S36; Details
FAQ
What is the role of 1-(9H-Fluoren-9-ylmethoxy)carbonyl)proline in chemical research?

1-(9H-Fluoren-9-ylmethoxy)carbonyl)proline, also known as Fmoc-Proline, is widely used in chemical research as a protecting group for amino acids. It is commonly utilized in peptide synthesis to prevent unwanted reactions and ensure the successful completion of the peptide chain.

How does Fmoc-Proline differ from other protecting groups in peptide synthesis?

Fmoc-Proline offers several advantages over other protecting groups in peptide synthesis. It is easily removed under mild conditions, making it a popular choice for peptide chemists. Additionally, Fmoc-Proline provides high selectivity and stability during the synthesis process, leading to efficient and reliable results.

What are the key applications of 1-(9H-Fluoren-9-ylmethoxy)carbonyl)proline in the pharmaceutical industry?

In the pharmaceutical industry, Fmoc-Proline is commonly used in the synthesis of peptide-based drugs and drug delivery systems. Its high selectivity and compatibility with various synthetic methods make it an essential building block for the production of bioactive peptides with therapeutic potential.

How can researchers benefit from using Fmoc-Proline in their peptide synthesis projects?

By using Fmoc-Proline in peptide synthesis projects, researchers can streamline the synthesis process, reduce side reactions, and improve the overall efficiency of peptide production. Its ease of use, selectivity, and stability make it a valuable tool for achieving high-quality peptide sequences in a cost-effective manner.

What are some best practices for handling and storing 1-(9H-Fluoren-9-ylmethoxy)carbonyl)proline in the laboratory?

When working with Fmoc-Proline in the laboratory, it is important to handle the compound with care to avoid exposure to skin and eyes. Proper storage in a cool, dry place away from light and moisture is essential to maintain the stability and integrity of the compound. Additionally, researchers should follow recommended safety protocols and wear appropriate protective gear when working with Fmoc-Proline.
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