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Merck

47636

Sigma-Aldrich

Fmoc-Pro-OH

≥90% (HPLC)

Synonym(e):

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

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About This Item

Empirische Formel (Hill-System):
C20H19NO4
CAS-Nummer:
Molekulargewicht:
337.37
Beilstein:
3596735
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352209
eCl@ss:
32160406
PubChem Substanz-ID:
NACRES:
NA.26

Qualitätsniveau

Assay

≥90% (HPLC)

Optische Aktivität

[α]20/D −32±1°, c = 1% in DMF

Eignung der Reaktion

reaction type: Fmoc solid-phase peptide synthesis

mp (Schmelzpunkt)

117-118 °C (lit.)

Anwendung(en)

peptide synthesis

Funktionelle Gruppe

Fmoc

Lagertemp.

2-8°C

SMILES String

OC(=O)[C@@H]1CCCN1C(=O)OCC2c3ccccc3-c4ccccc24

InChI

1S/C20H19NO4/c22-19(23)18-10-5-11-21(18)20(24)25-12-17-15-8-3-1-6-13(15)14-7-2-4-9-16(14)17/h1-4,6-9,17-18H,5,10-12H2,(H,22,23)/t18-/m0/s1

InChIKey

ZPGDWQNBZYOZTI-SFHVURJKSA-N

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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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Proline analogues are promising candidates for tuning the biological, pharmaceutical, or physicochemical properties of naturally occuring, as well as de novo designed, linear, and, cyclic peptides.

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

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

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