| Identification | Back Directory | [Name]
BOC-TRP(BOC)-OH | [CAS]
144599-95-1 | [Synonyms]
BOC-TRP(BOC)-OH
BOC-L-TRP(BOC)-OH
BOC-TRYPTOPHAN(BOC)-OH
N,1-bis-Boc-L-tryptophan
BOC-TRP(BOC)-OH USP/EP/BP
BOC-N-IN-BOC-L-TRYPTOPHAN
N-Boc-N'-Boc-L-tryptophan
Nα-Boc-Nin-Boc-L-tryptophan
Nalpha,1-Di-Boc-L-tryptophan
N-Boc-1-Boc-L-tryptophan,95%
N-Boc-1-Boc-L-tryptophan, 95%
N-α-Boc-N-in-Boc-L-tryptophan
Nα-Boc-Nin-Boc-L-tryptophan99%
(Tert-Butoxy)Carbonyl Trp(Boc)-OH
N-.ALPHA.-BOC-N-IN-BOC-L-TRYPTOPHAN
N-ALPHA-T-BOC-N-IN-T-BOC-L-TRYPOPHAN
N,N'-DI-(T-BUTYLOXYCARBONYL)-L-TRYPTOPHANE
N,N'-DI-TERT-BUTYLOXYCARBONYL-L-TRYPTOPHAN
N-α-tert-Butoxycarbonyl-N(in)-Boc-L-tryptophan
N,1-Bis[(1,1-dimethylethoxy)carbonyl]-L-tryptophan
L-Tryptophan, N,1-bis[(1,1-dimethylethoxy)carbonyl]-
N-ALPHA-T-BUTYLOXYCARBONYL-N-IN-T-BUTOXYCARBONYL-L-TRYPTOPHAN
(S)-3-(1-(tert-butoxycarbonyl)-1H-indol-3-yl)-2-(tert-butoxycarbonylamino)propanoic acid
(2S)-3-{1-[(tert-butoxy)carbonyl]-1H-indol-3-yl}-2-{[(tert-butoxy)carbonyl]amino}propanoic acid
2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-3-[1-[(2-methylpropan-2-yl)oxy-oxomethyl]-3-indolyl]propanoic acid | [Molecular Formula]
C21H28N2O6 | [MDL Number]
MFCD00270520 | [MOL File]
144599-95-1.mol | [Molecular Weight]
404.46 |
| Chemical Properties | Back Directory | [density ]
1.20±0.1 g/cm3(Predicted) | [storage temp. ]
-20°C | [solubility ]
Soluble in dimethylformamide (1 mmole in 2 ml). | [form ]
powder | [pka]
3.82±0.10(Predicted) | [Appearance]
White to light yellow Solid | [Optical Rotation]
-9.7°(C=0.01 g/ml DMF) | [Major Application]
peptide synthesis | [InChI]
1S/C21H28N2O6/c1-20(2,3)28-18(26)22-15(17(24)25)11-13-12-23(19(27)29-21(4,5)6)16-10-8-7-9-14(13)16/h7-10,12,15H,11H2,1-6H3,(H,22,26)(H,24,25)/t15-/m0/s1 | [InChIKey]
FATGZMFSCKUQGO-HNNXBMFYSA-N | [SMILES]
[n]1(c2c(c(c1)C[C@H](NC(=O)OC(C)(C)C)C(=O)O)cccc2)C(=O)OC(C)(C)C |
| Hazard Information | Back Directory | [Uses]
N-Boc-1-Boc-L-tryptophan is generally used as a intermediate in pharmaceutical and chemical research. | [reaction suitability]
reaction type: Boc solid-phase peptide synthesis |
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