| 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 |
| Chemical Properties | Back Directory | [Appearance]
Off-white powder | [Boiling point ]
488.0±40.0 °C(Predicted) | [density ]
1.290±0.06 g/cm3(Predicted) | [storage temp. ]
Store at R.T. | [form ]
solid | [pka]
3.69±0.11(Predicted) | [Major Application]
peptide synthesis | [InChI]
1S/C14H18N2O6/c1-14(2,3)22-13(19)15-10(12(17)18)8-9-6-4-5-7-11(9)16(20)21/h4-7,10H,8H2,1-3H3,(H,15,19)(H,17,18)/t10-/m0/s1 | [InChIKey]
BSHMNGMAJNWNBP-JTQLQIEISA-N | [SMILES]
OC([C@@H](NC(OC(C)(C)C)=O)CC1=C([N+]([O-])=O)C=CC=C1)=O | [CAS DataBase Reference]
185146-84-3(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [WGK Germany ]
WGK 3 | [HazardClass ]
IRRITANT | [HS Code ]
2922498590 | [Storage Class]
11 - Combustible Solids |
| 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. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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