ChemicalBook--->CAS DataBase List--->143415-63-8

143415-63-8

143415-63-8 Structure

143415-63-8 Structure
IdentificationBack Directory
[Name]

Boc-2-Methoxy-L-Phenylalanine
[CAS]

143415-63-8
[Synonyms]

Boc-L-Phe(2-OMe)-OH
Boc-2-Methoxy-L-Phenylalanine
Boc-2-methoxy-L-phenylalanine 97%
(Tert-Butoxy)Carbonyl 2-Methoxy-L-Phenylalanine
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-2-methoxy-
(S)-2-TERT-BUTHOXYCARBONYLAMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID
(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-methoxyphenyl)propanoic acid
(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(2-methoxyphenyl)propanoic acid
[Molecular Formula]

C15H21NO5
[MDL Number]

MFCD01860640
[MOL File]

143415-63-8.mol
[Molecular Weight]

295.33
Chemical PropertiesBack Directory
[Melting point ]

157°C
[Boiling point ]

451.664±40.00 °C(Press: 760.00 Torr)(predicted)
[density ]

1.169±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
[storage temp. ]

2-8°C
[form ]

powder
[pka]

3.956±0.11(predicted)
[color ]

White to off-white
[Major Application]

peptide synthesis
[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
[InChIKey]

QMHKMTAKTUUKEK-NSHDSACASA-N
[SMILES]

OC([C@@H](NC(OC(C)(C)C)=O)CC1=CC=CC=C1OC)=O
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P305+P351+P338-P337+P313-P261-P271-P304+P340-P312-P403+P233-P405-P501
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

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).
[reaction suitability]

reaction type: Boc solid-phase peptide synthesis
reagent type: ligand
reaction type: C-H Activation
Spectrum DetailBack Directory
[Spectrum Detail]

Boc-2-Methoxy-L-Phenylalanine(143415-63-8)1HNMR
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