CAS 86060-86-8
:fmoc-L-alanine pentafluorophenyl ester
Description:
Fmoc-L-alanine pentafluorophenyl ester is a chemical compound commonly used in peptide synthesis and organic chemistry. It features the Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is widely utilized to protect amino groups during peptide formation. The presence of the pentafluorophenyl ester moiety enhances the reactivity of the carboxylic acid, facilitating the formation of peptide bonds. This compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and dimethylformamide. Its structure includes a phenyl ring substituted with five fluorine atoms, which contributes to its unique chemical properties, including increased lipophilicity and stability. Fmoc-L-alanine pentafluorophenyl ester is valued for its ability to provide selective protection and activation of amino acids, making it a crucial reagent in the synthesis of peptides and other complex organic molecules. Proper handling and storage are essential, as with many fluorinated compounds, due to potential toxicity and environmental concerns.
Formula:C24H16F5NO4
InChI:InChI=1/C24H16F5NO4/c1-11(23(31)34-22-20(28)18(26)17(25)19(27)21(22)29)30-24(32)33-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16H,10H2,1H3,(H,30,32)/t11-/m0/s1
SMILES:C[C@@H](C(=O)Oc1c(c(c(c(c1F)F)F)F)F)N=C(O)OCC1c2ccccc2c2ccccc12
Synonyms:- Fmoc-Ala-OPfp
- N-alpha-(9-fluorenylmethyloxycarbonyl)-L-alanine pentafluorphenyl ester
- pentafluorophenyl N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alaninate
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Found 6 products.
Fmoc-Ala-OPfp
CAS:<p>Bachem ID: 4011871.</p>Formula:C24H16F5NO4Purity:99.7%Color and Shape:WhiteMolecular weight:477.39Fmoc-L-alanine pentafluorophenyl ester
CAS:<p>Fmoc-L-alanine pentafluorophenyl ester is a drug that inhibits the growth of microorganisms by inhibiting the synthesis of folic acid. It is used to treat patients with drug-resistant bacteria, such as Mycobacterium tuberculosis, and has shown toxic effects on human cells. Fmoc-L-alanine pentafluorophenyl ester binds to the enzyme dihydrofolate reductase and blocks the production of tetrahydrofolate, which is essential for DNA synthesis. This drug also inhibits human cells by binding to DNA gyrase in the bacterial cell wall.END></p>Formula:C24H16F5NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:477.38 g/mol





