ALD00352
Boc-2-methoxy-L-phenylalanine
97%
别名:
(S)-2-(tert-butoxycarbonylamino)-3-(2-methoxyphenyl)propanoic acid
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关于此项目
经验公式（希尔记法）:
C15H21NO5
化学文摘社编号:
分子量:
295.33
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
InChI key
QMHKMTAKTUUKEK-NSHDSACASA-N
SMILES string
OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1OC)=O
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
assay
97%
form
powder
reaction suitability
reaction type: Boc solid-phase peptide synthesis, reagent type: ligand
reaction type: C-H Activation
mp
157 °C
application(s)
peptide synthesis
storage temp.
2-8°C
Quality Level
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).
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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