Boc-2-methoxy-ʟ-phenylalanine, 1 X 1 g (ALD00352-1G)

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ALD00352-1G

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

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form	powder
InChI key	QMHKMTAKTUUKEK-NSHDSACASA-N
application(s)	peptide synthesis
assay	97%
reaction suitability	reaction type: Boc solid-phase peptide synthesis
storage temp.	2-8°C
Quality Level	100
InChI	1S/C15H21NO5/c1-15(2,3)21-14(19)16-11(13(17)18)9-10-7-5-6-8-12(10)20-4/h5-8,11H,9H2,1-4H3,(H,16,19)(H,17,18)/t11-/m0/s1
CAS_NO	143415-63-8
reaction suitability	reagent type: ligandreaction type: C-H Activation
SMILES string	OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1OC)=O
mp	157 °C

Boc-2-methoxy-ʟ-phenylalanine, 1 X 1 g (ALD00352-1G)

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Boc-2-methoxy-ʟ-phenylalanine, 1 X 1 g (ALD00352-1G)

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