Boc-2-methoxy-L-phenylalanine

ALDRICH/ALD00352 - 97%

Synonym: (S)-2-(tert-butoxycarbonylamino)-3-(2-methoxyphenyl)propanoic acid

CAS Number: 143415-63-8
Empirical Formula (Hill Notation): C₁₅H₂₁NO₅
Molecular Weight: 295.33
MDL Number: MFCD01860640
Linear Formula: C₁₅H₂₁NO₅
Product Type: Chemical

Catalog Number	PKG Qty.	Price


45-ALD00352-1G	1 g	$273.00 1/EA	Add To Favorites

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Properties
Descriptions
Safety Info.
Basic Data

application(s)	peptide synthesis
assay	97%
form	powder
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
InChI key	QMHKMTAKTUUKEK-NSHDSACASA-N
mp	157 °C
Quality Level	100
reaction suitability	reaction type: Boc solid-phase peptide synthesis
	reagent type: ligand reaction type: C-H Activation
SMILES string	OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1OC)=O
storage temp.	2-8°C

Application:	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).
Other Notes:	Ligand-Controlled C(sp³)–H Arylation and Olefination in Synthesis of Unnatural Chiral α–Amino Acids
Packaging:	1 g in glass bottle

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Purity	97%
mp	157 °C
Storage Temp.	2-8°C
UNSPSC	12352209

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