Fmoc-Val-OH
- Molecular formula
- C22H23NO4
- CAS Number
- 68858-19-1
- IUPAC Name
- 2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methyl-pentanoic acid
- Molecular Weight
- 373.44g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2890g/cm3
- Synonyms
- DL-LEUCINE-D10-N-FMOC
Identification
Interesting Facts about 2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methyl-pentanoic acid
This compound, often referred to as a protecting group in organic synthesis, plays a crucial role in peptide synthesis and other complex organic transformations. Its structure features a fluorene moiety, which contributes to its stability and functionality. Here are some engaging aspects of this compound:
- Protective Functionality: The 9H-fluoren-9-ylmethoxycarbonyl (Fmoc) group is widely used in solid-phase peptide synthesis. It offers a way to protect amino groups, allowing for selective reactions.
- Versatile Applications: This compound is not only important in peptide synthesis but also in the design of novel pharmaceuticals and bioactive molecules.
- Enhanced Stability: The fluorene structure contributes to the compound's photophysical properties, making it highly stable under various conditions, which is essential for laboratory manipulations.
- Derivative Potential: By modifying the side groups, chemists can create a variety of derivatives, expanding the utility of this compound in scientific research.
- Interaction with Biological Systems: Its structure can influence interactions with biological molecules, making it a point of interest for biochemical studies.
In the words of a renowned chemist, “The beauty of organic synthesis lies in the ability to construct complex molecules through strategic planning and the use of protecting groups.” This compound exemplifies that beauty, enabling chemists to achieve intricate molecular architectures!
Whether you are a linear thinker or a creative problem solver, the multifunctionality of this compound opens up an exciting realm of possibilities in organic chemistry!