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Merck

47638

Sigma-Aldrich

Fmoc-Val-OH

≥98.0% (HPLC)

Synonym(e):

N-(Fluorenyl-9-methoxycarbonyl)-L-valin, Fmoc-L-valin

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About This Item

Empirische Formel (Hill-System):
C20H21NO4
CAS-Nummer:
Molekulargewicht:
339.39
Beilstein:
2177443
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352209
eCl@ss:
32160406
PubChem Substanz-ID:
NACRES:
NA.26

Qualitätsniveau

Assay

≥98.0% (HPLC)

Form

solid

Optische Aktivität

[α]20/D −17±1°, c = 1% in DMF

Eignung der Reaktion

reaction type: C-H Activation
reaction type: Fmoc solid-phase peptide synthesis
reagent type: ligand
reaction type: Peptide Synthesis

mp (Schmelzpunkt)

143-145 °C (lit.)
143-147 °C

Anwendung(en)

peptide synthesis

Funktionelle Gruppe

Fmoc
amine
carboxylic acid

Lagertemp.

2-8°C

SMILES String

CC(C)[C@H](NC(=O)OCC1c2ccccc2-c3ccccc13)C(O)=O

InChI

1S/C20H21NO4/c1-12(2)18(19(22)23)21-20(24)25-11-17-15-9-5-3-7-13(15)14-8-4-6-10-16(14)17/h3-10,12,17-18H,11H2,1-2H3,(H,21,24)(H,22,23)/t18-/m0/s1

InChIKey

UGNIYGNGCNXHTR-SFHVURJKSA-N

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Allgemeine Beschreibung

Fmoc-Val-OH also known as Fmoc-L-valine, is a versatile reagent used in the Fmoc Solid-phase peptide synthesis.

Anwendung

Fmoc-Val-OH can be used as a starting material to synthesize:
  • difficult sequence-containing pentapeptides using O-acyl isodipeptide unit
  • peptides by backbone amide linker (BAL) strategy via Fmoc Solid-phase synthesis

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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With a growing peptide drug market the fast, reliable and uncomplicated synthesis of peptides is of paramount importance.

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