Taiy Chemical
1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione
Product Name N-(9-Fluorenylmethoxycarbonyloxy)succinimide
Synonyms:89706 1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione; FMOC-ONSu; N-(9-fluorenylmethoxycarbonyloxy)-succinimide; N-(9-Fluorenylmethyloxycarbonyl) oxysuccinimide; N-(9H-Fluoren-2-ylmethoxycarbonyloxy)succinimide; FMOC-OSU; N-(9-Fluorenylmethoxy Carbonyloxy) succinimide; 9-Fluorenylmethyl succinimidyl carbonate; 1-{[(9H-fluoren-9-ylmethoxy)carbonyl]oxy}pyrrolidine-2,5-dione; N-(9-Fluorenylmethoxy-carbonyloxy)succinimide; N-(9-Fluorenylmethoxy Carbonyloxy)Succinimide; N-(9-FluorenylmethoxyCarbonyloxy) Succinimide
CAS RN. 82911-69-1
EINECS 433-520-5
Molecular Weight 337.3261
Molecular Formula C19H15NO5
Density 1.42g/cm3
Melting Point(℃) 150-153℃
Boiling Point(℃) 494.3°C at 760 mmHg
Flash Point(℃) 252.7°C
refractive_index 1.661
Hazard Symbols Xi Details
Xi
Risk Codes  R36/37/38;    Details
 R36/37/38;     Details
Safety Description  S24/25;Details
 S24/25; Details
FAQ
What is 1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione (Fmoc-5Pyr)?
1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione, also known as Fmoc-5Pyr, is a chemical compound commonly used in organic synthesis and peptide chemistry. It is an important reagent for protecting amino groups during peptide synthesis and can be used for the solid-phase peptide synthesis of various peptides and proteins.

How is 1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione (Fmoc-5Pyr) typically used in peptide synthesis?
Fmoc-5Pyr is commonly used as a protecting group reagent for the amino groups of amino acids during solid-phase peptide synthesis. By attaching the Fmoc-5Pyr group to the N-terminus of the growing peptide chain, it prevents unwanted side reactions and ensures selective deprotection of the amino group during subsequent synthesis steps.

What are the benefits of using 1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione (Fmoc-5Pyr) in peptide synthesis?
Some of the benefits of using Fmoc-5Pyr in peptide synthesis include:
1. Selective protection of amino groups: Fmoc-5Pyr provides a high degree of selectivity in protecting amino groups, which helps to avoid unwanted side reactions.
2. Compatibility with solid-phase synthesis: Fmoc-5Pyr is well-suited for solid-phase peptide synthesis, making it a versatile reagent for the synthesis of peptides and proteins.
3. Mild deprotection conditions: Fmoc-5Pyr can be readily deprotected under mild conditions, allowing for efficient and reliable peptide synthesis.
4. High purity and yield: Fmoc-5Pyr reagents are known for their high purity and yield, ensuring the quality of synthesized peptides.

Are there any considerations or precautions to be aware of when using 1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione (Fmoc-5Pyr)?
When working with Fmoc-5Pyr in peptide synthesis, it is important to consider the following precautions:
1. Use appropriate safety measures: Handle Fmoc-5Pyr reagents with care and follow all recommended safety guidelines to ensure safe handling.
2. Storage conditions: Store Fmoc-5Pyr reagents in a cool, dry place away from light and moisture to maintain their stability and effectiveness.
3. Compatibility with other reagents: Ensure that Fmoc-5Pyr is compatible with other reagents and solvents used in your peptide synthesis protocol to avoid any unexpected reactions or issues.
4. Quality of reagents: Use high-quality Fmoc-5Pyr reagents from reputable suppliers to ensure the success of your peptide synthesis experiments.

In conclusion, 1-(9H-Fluorenylmethoxycarbonyloxy)-2,5-pyrrolidinedione (Fmoc-5Pyr) is a valuable reagent for peptide synthesis, offering selective protection of amino groups, compatibility with solid-phase synthesis, mild deprotection conditions, and high purity and yield. By following proper safety precautions and considerations, researchers can effectively utilize Fmoc-5Pyr in their peptide synthesis projects to achieve reliable and high-quality results.
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