N-[(9 h-FLUOREN - 9-ylméthoxy)carbonyle]-2 m

Code: ald00350-1g D2-231

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Unnatrual amino acid was derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. The Pd-mediated C-C bond formation can be made in tande...


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Votre prix
$317.70 1G
DEMANDER

Non disponible en dehors du Royaume-Uni et de l'Irlande

Application

Unnatrual amino acid was derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. The Pd-mediated C-C bond formation can be made in tandem with 2-Methylpyridine (Aldrich 109835).

Other Notes

Ligand-Controlled C(sp3)–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids

Packaging

1 g in glass bottle

application(s)peptide synthesis
assay95% (HPLC)
formsolid
InChI keyCBCSNZJHURMDMO-QFIPXVFZSA-N
InChI1S/C25H23NO5/c1-30-23-13-7-2-8-16(23)14-22(24(27)28)26-25(29)31-15-21-19-11-5-3-9-17(19)18-10-4-6-12-20(18)21/h2-13,21-22H,14-15H2,1H3,(H,26,29)(H,27,28)/t22-/m0/s1
mp171-176 °C
Quality Level100
reaction suitabilityreaction type: solution phase peptide synthesis
SMILES stringOC([C@@H](NC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)CC4=CC=CC=C4OC)=O
storage temp.2-8°C
Cas Number206060-41-5
Ce produit répond aux critères suivants pour être admissible aux récompenses suivantes :



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