CAS 35661-40-6
:FMOC-L-fenilalanina
Descrição:
FMOC-L-fenilalanina, com o número CAS 35661-40-6, é um derivado do aminoácido fenilalanina, modificado com um grupo protetor de 9-fluorenilmetoxicarbonila (FMOC). Este composto é comumente utilizado na síntese de peptídeos, particularmente na síntese de peptídeos em fase sólida (SPPS), devido à sua capacidade de proteger o grupo amino da fenilalanina durante as reações de acoplamento. FMOC-L-fenilalanina é tipicamente um sólido branco a off-white e é solúvel em solventes orgânicos como dimetilformamida (DMF) e dimetilsulfóxido (DMSO), mas menos solúvel em água. O grupo FMOC pode ser removido em condições básicas suaves, permitindo a deproteção seletiva do grupo amino quando necessário. Este composto é valorizado por sua estabilidade e facilidade de manuseio, tornando-se uma escolha popular na síntese de peptídeos e outras moléculas orgânicas complexas. Além disso, mantém as propriedades biológicas da fenilalanina, que é essencial para vários processos metabólicos em organismos vivos.
Fórmula: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
Chave InChI: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
Sinónimos:- (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
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9 produtos.
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine
CAS:Fórmula:C24H21NO4Pureza:>98.0%(T)(HPLC)Cor e Forma:White to Almost white powder to crystalPeso molecular:387.44Fmoc-Phe-OH
CAS:<p>Bachem ID: 4100450.</p>Fórmula:C24H21NO4Pureza:99.9%Cor e Forma:White PowderPeso molecular:387.44Ref: IN-DA00I72V
5g20,00€10g24,00€1kg222,00€25g28,00€50g41,00€5kgA consultar100g55,00€10kgA consultar250g108,00€500g159,00€FMOC-Phe-OH
CAS:FMOC-Phe-OHFórmula:C24H21NO4Pureza:98.91%Cor e Forma: white powderPeso molecular: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>Fórmula:C24H21NO4Pureza:Min. 98.0 Area-%Peso molecular: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>Fórmula:C24H21NO4Pureza:Min. 98 Area-%Cor e Forma:White Off-White PowderPeso molecular:387.43 g/molFmoc-Phe-OH
CAS:<p>M03370 - Fmoc-Phe-OH</p>Fórmula:C24H21NO4Pureza:99%Cor e Forma:Solid, Chunks or Crystalline PowderPeso molecular:387.435FMOC-L-Phenylalanine extrapure, 99%
CAS:Fórmula:C24H21NO4Pureza:min. 99%Cor e Forma:White, Crystalline powderPeso molecular:387.40







