CAS 35661-40-6
:FMOC-L-phenylalanine
Description:
FMOC-L-phenylalanine, with the CAS number 35661-40-6, is a derivative of the amino acid phenylalanine, modified with a 9-fluorenylmethoxycarbonyl (FMOC) protecting group. This compound is commonly used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), due to its ability to protect the amino group of phenylalanine during the coupling reactions. FMOC-L-phenylalanine is typically a white to off-white solid and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. The FMOC group can be removed under mild basic conditions, allowing for the selective deprotection of the amino group when needed. This compound is valued for its stability and ease of handling, making it a popular choice in the synthesis of peptides and other complex organic molecules. Additionally, it retains the biological properties of phenylalanine, which is essential for various metabolic processes in living organisms.
Formula:C24H21NO4
InChI:InChI=1S/C24H21NO4/c26-23(27)22(14-16-8-2-1-3-9-16)25-24(28)29-15-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21/h1-13,21-22H,14-15H2,(H,25,28)(H,26,27)/t22-/m0/s1
InChI key:InChIKey=SJVFAHZPLIXNDH-QFIPXVFZSA-N
SMILES:C(OC(N[C@@H](CC1=CC=CC=C1)C(O)=O)=O)C2C=3C(C=4C2=CC=CC4)=CC=CC3
Synonyms:- (2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-phenylpropanoic acid
- (2S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]-3-phenylpropanoic acid
- (S)-2-[9H-Fluoren-9-yl(methoxycarbonyl)amino]-3-phenylpropionic acid
- (S)-N-Fmoc-phenylalanine
- 226: PN: US20070042401 PAGE: 30 claimed protein
- 3-fenil-N-[(9H-fluoren-9-ilmetoxi)carbonil]-L-alanina
- 917: PN: WO2006135786 PAGE: 59 claimed protein
- <span class="text-smallcaps">L</span>-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
- FMOC-<span class="text-smallcaps">L</span>-phenylalanine
- FMOC-L-phenylalanine
- Fmoc-phenylalanine
- N-(9-Fluorenylmethoxycarbonyl)-<span class="text-smallcaps">L</span>-phenylalanine
- N-(9-Fluorenylmethoxycarbonyl)-L-phenylalanine
- N-(9-Fluorenylmethoxycarbonyl)phenylalanine
- N-9-Fluorenylmethoxycarbonylphenylalanine
- N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-phenyl-L-alanin
- N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-phenylalanine
- N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
- N-[(9H-fluoren-9-ylmethoxy)carbonyl]-3-phenyl-L-alanine
- N-[(9H-fluorene-9-ylmethoxy)carbonyl]-3-phenyl-L-alanine
- N-α-[[(9H-Fluoren-9-yl)methoxy]carbonyl]-<span class="text-smallcaps">L</span>-phenylalanine
- Nsc 334293
- See more synonyms
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Found 9 products.
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
CAS:Formula:C24H21NO4Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:387.44Fmoc-Phe-OH
CAS:<p>Bachem ID: 4100450.</p>Formula:C24H21NO4Purity:99.9%Color and Shape:White PowderMolecular weight:387.44Ref: IN-DA00I72V
5g20.00€10g24.00€1kg222.00€25g28.00€50g41.00€5kgTo inquire100g55.00€10kgTo inquire250g108.00€500g159.00€FMOC-Phe-OH
CAS:FMOC-Phe-OHFormula:C24H21NO4Purity:98.91%Color and Shape: white powderMolecular weight:387.42784g/molFmoc-Phe-OH
CAS:<p>Fmoc-Phe-OH is a natural compound that has been shown to have antimicrobial properties. The biological properties of Fmoc-Phe-OH are not well understood, but it has been shown to have anticancer effects in some cases and to inhibit axonal growth when combined with the protein laminin. Fmoc-Phe-OH can be synthesized by the reaction of pheine with trifluoroacetic acid followed by treatment with h9c2 cells. The analytical method for determining the concentration of Fmoc-Phe-OH is based on intramolecular hydrogen exchange between hydrogen atoms on the amide group and hydrogens on neighboring methylene groups. This process releases heat, which is detected by a thermometer.<br>END></p>Formula:C24H21NO4Purity:Min. 98.0 Area-%Molecular weight:387.44 g/molFmoc-Phe-OH
CAS:<p>Fmoc-Phe-OH is an amino acid derivative that has been used as a fluorescence probe for the detection of cervical cancer. Fmoc-Phe-OH binds to the DNA of human cells, and its fluorescence properties change when it is exposed to hydroxyl groups in blood serum. In addition, Fmoc-Phe-OH can be synthesized by solid phase synthesis and this process is monitored by silver ions. The fluorescence properties of Fmoc-Phe-OH are sensitive to changes in morphology and phase transition temperature.</p>Formula:C24H21NO4Purity:Min. 98 Area-%Color and Shape:White Off-White PowderMolecular weight:387.43 g/molFmoc-Phe-OH
CAS:<p>M03370 - Fmoc-Phe-OH</p>Formula:C24H21NO4Purity:99%Color and Shape:Solid, Chunks or Crystalline PowderMolecular weight:387.435FMOC-L-Phenylalanine extrapure, 99%
CAS:Formula:C24H21NO4Purity:min. 99%Color and Shape:White, Crystalline powderMolecular weight:387.40







