Cookies disclaimer

I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.

71989-31-6 - N-Fmoc-L-proline, 98% - N-(9-Fluorenylmethoxycarbonyl)-L-proline - Fmoc-Pro-OH - B21081 - Alfa Aesar

B21081 N-Fmoc-L-proline, 98%

CAS-Nummer
71989-31-6
Synonyme
N-(9-Fluorenylmethoxycarbonyl)-L-proline
Fmoc-Pro-OH

SDS Analysenzertifikat Produktspezifikation Technische Anfrage
Größe Preis ($) Menge Verfügbarkeit
5g 57,90
25g 208,00
Zum Warenkorb hinzufügen Zur Angebotsanfrage hinzufügen Artikel anzeigen

N-Fmoc-L-proline, 98%

MDL
MFCD00037122
EINECS
276-259-0

Chemische Eigenschaften

Formel
C20H19NO4
Molmasse
337.38
Schmelzpunkt
113-117°
Löslichkeit
Soluble in methanol. (almost transparency.)

Anwendungen

It is used as pharmaceutical intermediate. Fmoc method is used for the synthesis of the new polymeric support for the preparation of C-terminal peptide amides.

Bemerkungen
Store at 2-8°C. Incompatible with oxidizing agents.

Literaturverweise

Peter Sieber. A new acid-labile anchor group for the solid-phase synthesis of C-terminal peptide amides by the Fmoc method. Tetrahedron Lett. 1987, 28 (19),2107-2110 .

Bin Zou.; Jingjun Wei.; Guorong Cai.; Dawei Ma. Synthesis of an Oxazoline Analogue of Apratoxin A. Org. Lett. 2003, 5 (19),3503-3506 .

Weitere Referenzen

Beilstein
3596735
Harmonized Tariff Code
2933.99
TSCA
No

Empfohlen

  • B21107
    N-Fmoc-L-alanine monohydrate, 98%

  • H26082
    O-(7-Aza-1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate, 99%

  • H50304
    N-Boc-1,3-diaminopropane, 95%

  • H59570
    N-Fmoc-D-valine, 98%

  • H62806
    N-Fmoc-N-methylglycine, 98%

Kürzlich angesehen

Chemikalien

Life science

Metalle und Stoffe

Katalysatoren

Forschungs- und Laborbedarf