CAS 35661-40-6

FMOC-L-fenilalanina

Descripción:

FMOC-L-fenilalanina, con el número CAS 35661-40-6, es un derivado del aminoácido fenilalanina, modificado con un grupo protector de 9-fluorenilmetoxicarbonilo (FMOC). Este compuesto se utiliza comúnmente en la síntesis de péptidos, particularmente en la síntesis de péptidos en fase sólida (SPPS), debido a su capacidad para proteger el grupo amino de la fenilalanina durante las reacciones de acilo. FMOC-L-fenilalanina es típicamente un sólido blanco a blanco sucio y es soluble en disolventes orgánicos como el dimetilformamida (DMF) y el dimetilsulfóxido (DMSO), pero menos soluble en agua. El grupo FMOC se puede eliminar en condiciones básicas suaves, permitiendo la deprotección selectiva del grupo amino cuando sea necesario. Este compuesto es valorado por su estabilidad y facilidad de manejo, lo que lo convierte en una opción popular en la síntesis de péptidos y otras moléculas orgánicas complejas. Además, conserva las propiedades biológicas de la fenilalanina, que es esencial para varios procesos metabólicos en los 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

Clave 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

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-phenylalanine

CAS: 35661-40-6

Fórmula: C₂₄H₂₁NO₄

Pureza: >98.0%(T)(HPLC)

Forma y color: White to Almost white powder to crystal

Peso molecular: 387.44

Ref: 3B-F0297

Fmoc-L-Phenylalanine

CAS: 35661-40-6

Fórmula: C₂₄H₂₁NO₄

Pureza: 98%

Forma y color: Solid

Peso molecular: 387.4278

Ref: IN-DA00I72V

Fmoc-Phe-OH

CAS: 35661-40-6

Fórmula: C₂₄H₂₁NO₄

Pureza: ≥ 99.0%

Forma y color: White powder

Peso molecular: 387.44

Ref: 7W-GM5097

Fmoc-Phe-OH

CAS: 35661-40-6

Fmoc-Phe-OH is a hydrophobic Fmoc-protected phenylalanine derivative, soluble in DMF/NMP, suitable for peptide synthesis and chemical biology research.

Fórmula: C₂₄H₂₁NO₄

Pureza: 99.96%

Forma y color: White Solid

Peso molecular: 387.43

Ref: TM-T67569

Fmoc-Phe-OH

CAS: 35661-40-6

Fmoc-Phe-OH

Fórmula: C₂₄H₂₁NO₄

Pureza: 98%

Peso molecular: 387.43

Ref: IN-DG8605

FMOC-Phe-OH

CAS: 35661-40-6

FMOC-Phe-OH

Fórmula: C₂₄H₂₁NO₄

Pureza: 98.91%

Forma y color: Solid-Powder

Peso molecular: 387.42784

Ref: 54-OR54571

Fmoc-Phe-OH

CAS: 35661-40-6

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.
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Fórmula: C₂₄H₂₁NO₄

Pureza: Min. 98.0 Area-%

Peso molecular: 387.44 g/mol

Ref: 3D-FLF-1730-PI

Fmoc-Phe-OH

CAS: 35661-40-6

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.

Fórmula: C₂₄H₂₁NO₄

Pureza: Min. 98 Area-%

Forma y color: White Off-White Powder

Peso molecular: 387.43 g/mol

Ref: 3D-FF15867

Fmoc-Phe-OH

CAS: 35661-40-6

M03370 - Fmoc-Phe-OH

Fórmula: C₂₄H₂₁NO₄

Pureza: 99%

Forma y color: Solid, Chunks or Crystalline Powder

Peso molecular: 387.435

Ref: 10-M03370

FMOC-L-Phenylalanine extrapure, 99%

CAS: 35661-40-6

Fórmula: C₂₄H₂₁NO₄

Pureza: min. 99%

Forma y color: White, Crystalline powder

Peso molecular: 387.40

Ref: SR-39061

Fmoc-Phe-OH

CAS: 35661-40-6

Bachem ID: 4100450.

Fórmula: C₂₄H₂₁NO₄

Pureza: 99.9%

Forma y color: White

Peso molecular: 387.44

Ref: 01-4100450