Identification | More | [Name]
L-2-NITROPHENYLALANINE | [CAS]
19883-75-1 | [Synonyms]
D-His(Trt) L-2-NITROPHE L-PHE(2-NO2) L-2-NO2-Phe-OH -2-NitrophenyL H-PHE(2-NO2)-OH H-O-NITRO-PHE-OH L-2-NITROPHENYLALANINE 2-NITRO-L-PHENYLALANINE L-Phenylalanine, 2-nitro- L-2-NO2-Phe-OH 2-Nitro-L-Phenylalanine (S)-2-AMino-3-(2-nitrophenyl)propanoic acid L-2-AMINO-3-(2-NITRO PHENYL)-PROPIONIC ACID (2S)-2-amino-3-(2-nitrophenyl)propanoic acid | [Molecular Formula]
C9H10N2O4 | [MDL Number]
MFCD00270360 | [Molecular Weight]
210.19 | [MOL File]
19883-75-1.mol |
Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H319-H335 | [Precautionary statements ]
P261-P271-P280 | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . |
Hazard Information | Back Directory | [Uses]
L-2-Nitrophenylalanine is a 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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