High-Purity 9-Fluorenemethanol (CAS 24324-17-2): A Key Reagent in Peptide Synthesis and Organic Chemistry

Discover the crucial role of 9-Fluorenemethanol in advancing modern chemistry and biological research.

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Key Advantages

Versatile Protecting Group Strategy

The ability of 9-fluorenemethanol to act as both a carboxy and phosphate protecting group makes it a highly versatile tool, simplifying complex synthetic pathways in both peptide and oligonucleotide research.

Controlled Cleavage

A significant advantage of 9-fluorenemethanol is that the 9-fluorenylmethyl esters it forms can be readily cleaved using mild basic conditions, such as with piperidine, allowing for selective deprotection without damaging the desired product.

High Purity and Reliability

Sourced with precision, this compound, identified by CAS 24324-17-2, is often supplied in high purity, which is critical for achieving reliable and reproducible results in sensitive chemical and biological synthesis.

Key Applications

Peptide Synthesis

9-fluorenemethanol is fundamental in preparing 9-fluorenylmethyl esters, which are essential for protecting amino acid carboxyl groups during peptide chain elongation.

Oligonucleotide Synthesis

Its role as a phosphate protecting group is critical in the step-by-step synthesis of DNA and RNA fragments, ensuring the accuracy of the genetic code.

Organic Synthesis

Beyond biological applications, it serves as a valuable building block and reagent in various complex organic transformations, offering selective protection strategies.

Research and Development

Academic and industrial researchers rely on 9-fluorenemethanol for developing new synthetic methodologies and exploring novel chemical structures.