Taiy Chemical
1-[(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid
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 primary function of [1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid?

[1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid is primarily used as a chemical reagent in various organic synthesis reactions. It serves as a building block in the preparation of complex molecules in pharmaceutical research, agrochemicals, and materials science.

How is [1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid synthesized?

The synthesis of [1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid typically involves the reaction of fluorenylmethoxycarbonyl chloride with pyrrolidine-2-carboxylic acid. This reaction results in the formation of the desired compound through a series of purification and isolation steps.

What are the key features of [1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid in terms of its chemical properties?

[1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid is a white to off-white solid with a high melting point. It is sparingly soluble in common organic solvents such as methanol and acetonitrile. The compound is relatively stable under standard lab conditions and is commonly used in peptide chemistry due to its protecting group capabilities.

How is [1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid utilized in the field of drug discovery?

In drug discovery, [1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid plays a crucial role as a protecting group for amino acids during peptide synthesis. This compound enables chemists to control the reactivity of amino acids and selectively activate specific functional groups, facilitating the formation of desired peptide sequences with high precision.

What are the storage and handling considerations for [1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid?

[1-(9H-fluoren-9-ylmethoxy)carbonyl]pyrrolidine-2-carboxylic acid should be stored in a cool, dry place away from direct sunlight and sources of heat. It is recommended to keep the compound tightly sealed in its original container to prevent moisture absorption and contamination. Proper handling procedures, including the use of appropriate personal protective equipment, should be followed to minimize the risk of exposure and ensure safety in the laboratory environment.
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