Boc-3-[3,4-bis(trifluoromethyl)phenyl]-ʟ-alanine, 1 X 1 g (ALD00348-1G)

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ALD00348-1G

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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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SDS

storage temp.	2-8°C
form	powder or solid
assay	≥95% (HPLC)
application(s)	peptide synthesis
reaction suitability	reaction type: Boc solid-phase peptide synthesis
reaction suitability	reagent type: ligandreaction type: C-H Activation
description	ALPH: +24.0, 0.5%EtOH
SMILES string	OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC(C(F)(F)F)=C(C(F)(F)F)C=C1)=O
InChI	1S/C16H17F6NO4/c1-14(2,3)27-13(26)23-11(12(24)25)7-8-4-5-9(15(17,18)19)10(6-8)16(20,21)22/h4-6,11H,7H2,1-3H3,(H,23,26)(H,24,25)/t11-/m0/s1
CAS_NO	2120095-23-8
InChI key	LLRXWQAYIGATCH-NSHDSACASA-N
Quality Level	100

Boc-3-[3,4-bis(trifluoromethyl)phenyl]-ʟ-alanine, 1 X 1 g (ALD00348-1G)

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Boc-3-[3,4-bis(trifluoromethyl)phenyl]-ʟ-alanine, 1 X 1 g (ALD00348-1G)

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