| Identification | More | [Name]
BOC-D-4-Nitrophe | [CAS]
61280-75-9 | [Synonyms]
BOC-4-NITRO-D-PHENYLALANINE BOC-4-NITRO-D-PHE-OH BOC-D-4-NITROPHE BOC-D-4-NITROPHENYLALANINE BOC-D-PHE(4-NO2)-OH BOC-D-PHE(P-NO2) BOC-D-(P-NO2)PHE-OH BOC-P-NITRO-D-PHENYLALANINE BOC-P-NITRO-D-PHE-OH BOC-PNO2-D-PHE-OH N-ALPHA-T-BOC-4-NITRO-D-PHENYLALANINE N-ALPHA-T-BUTOXYCARBONYL-P-NITRO-D-PHENYLALANINE N-ALPHA-TERT-BUTYLOXYCARBONYL-D-4-NITROPHENYLALANINE N-TBOC-P-NITRO-D-PHENYLALANINE N-T-BUTOXYCARBONYL-4-NITRO-D-PHENYLALANINE (R)-2-(TERT-BUTOXYCARBONYLAMINO)-3-(4-NITROPHENYL)PROPANOIC ACID RARECHEM BK PT 0077 tert-butoxycarbonyl-d-4-nitrophenylalanine N-T-BOC-P-NITRO-D-PHENYLALANINE*FREE ACI D 4-Nitro-D-phenylalanine, N-BOC protected | [Molecular Formula]
C14H18N2O6 | [MDL Number]
MFCD00069880 | [Molecular Weight]
310.3 | [MOL File]
61280-75-9.mol |
| Chemical Properties | Back Directory | [Melting point ]
120°C | [alpha ]
-8 º (c=1,MeOH) | [Boiling point ]
509.3±45.0 °C(Predicted) | [density ]
1.290±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C
| [solubility ]
soluble in Methanol | [form ]
powder to crystal | [pka]
3.70±0.10(Predicted) | [color ]
White to Light yellow | [BRN ]
4203814 | [Major Application]
peptide synthesis | [InChI]
1S/C14H18N2O6/c1-14(2,3)22-13(19)15-11(12(17)18)8-9-4-6-10(7-5-9)16(20)21/h4-7,11H,8H2,1-3H3,(H,15,19)(H,17,18)/t11-/m1/s1 | [InChIKey]
XBQADBXCNQPHHY-LLVKDONJSA-N | [SMILES]
CC(C)(C)OC(=O)N[C@H](Cc1ccc(cc1)[N+]([O-])=O)C(O)=O | [CAS DataBase Reference]
61280-75-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Safety Statements ]
24/25 | [WGK Germany ]
3
| [F ]
8 | [HazardClass ]
IRRITANT | [HS Code ]
29242990 | [Storage Class]
11 - Combustible Solids |
| Hazard Information | Back Directory | [Chemical Properties]
White powder | [Uses]
N-Boc-p-nitro-D-phenylalanine is the N-Boc protected form of p-Nitro-D-phenylalanine (N502720). Also a useful synthetic intermediate in the synthesis of (R)-Hydroxymelphalan (H393845, TFA salt); an analog of Melphalan (M216900) which is an antineoplastic. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
|
|