| Identification | More | [Name]
BOC-L-2-NITROPHENYLALANINE | [CAS]
185146-84-3 | [Synonyms]
BOC-L-PHE(2-NO2)
BOC-L-2-NITROPHE
BOC-PHE(2-NO2)-OH
Boc-L-2-NO2-Phe-OH
BOC-L-2-NITROPHENYLALANINE
BOC-2-NITRO-L-PHENYLALANINE
(Tert-Butoxy)Carbonyl L-2-Nitrophe
2-Nitro-L-phenylalanine, N-BOC protected
N-α-(t-Butoxycarbonyl)-2-nitro-L-phenylalanine
Boc-L-2-NO2-Phe-OH Boc-2-Nitro-L-Phenylalanine
N-[(1,1-Dimethylethoxy)carbonyl]-2-nitro-L-phenylalanine
L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-2-nitro-
(S)-2-(tert-butoxycarbonylamino)-3-(2-nitrophenyl)propanoic acid
(S)-N-ALPHA-T-BUTOXYCARBONYL-2-AMINO-3-(2-NITRO-PHENYL)-PROPANOIC ACID
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-(2-nitrophenyl)propanoic acid | [Molecular Formula]
C14H18N2O6 | [MDL Number]
MFCD01317708 | [Molecular Weight]
310.3 | [MOL File]
185146-84-3.mol |
| Hazard Information | Back Directory | [Chemical Properties]
Off-white powder | [Uses]
Boc-L-2-Nitrophenylalanine is a protected derivative of L-Phenylalanine (P319415), and is used in the photocleavage of polypeptide backbones. L-Phenylalanine is an essential amino acid. L-Phenylalanine is biologically converted into L-tyrosine, another one of the DNA-encoded amino acids, which in turn is converted to L-DOPA and further converted into dopamine, norepinephrine, and epinephrine. |
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