| Identification | Back Directory | [Name]
FMOC-DPR(BOC-AOA)-OH | [CAS]
600153-12-6 | [Synonyms]
FMOC-L-DAP(BOC-AOA)
FMOC-DAP(BOC-AOA)-OH
FMOC-DPR(BOC-AOA)-OH
FMOC-L-DAP(BOC-AOA)-OH
FMOC-L-DAPA(BOC-AOA)-OH
FMOC-DPR(BOC-AOA)-OH 1 G
FMOC-DAP[AC(-O-NHBOC)]-OH
Nα-Fmoc-Nβ-(N-Boc-amino-oxyacetyl)-L-2,3-diaminopropionic acid
(S)-2-(Fmoc-amino)-3-[2-(Boc-aminooxy)acetamido]propanoic acid
N-ALPHA-FMOC-N-BETA-(BOC-AMINOOXYACETYL)-L-DIAMINOPROPIONIC ACID
N-ALPHA-FMOC-N-BETA-(N-T-BOC-AMINO-OXYACETYL)-L-DIAMINOPROPIONIC ACID
N-ALPHA-FMOC-N-BETA-(N-T-BOC-AMINO-OXYACETYL)-L-2,3-DIAMINOPROPIONIC ACID
Nα-Fmoc-Nβ-(N-Boc-amino-oxyacetyl)-L-2,3-diaminopropionic acid≥ 98% (HPLC)
Nα-FMoc-Nβ-(N-Boc-aMino-oxyacetyl)-L-2,3-diaMinopropionic acid
N-α-(9-Fluorenylmethoxycarbonyl)-N-β-[(t-butoxycarbonyl)-aminooxyacetyl]-L-α,β-diaminopropionic acid
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-BETA-(T-BUTOXYCARBONYL-AMINOOXYACETYL)-L-2,3-DIAMINOPROPIONIC ACID
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-BETA-(T-BUTYLOXYCARBONYL-AMINOOXY-ACETYL)-L-2,3-DIAMINOPROPIONIC ACID
(8S)-1-(1,1-dimethylethyl) 10-(9H-fluoren-9-ylmethyl) ester, 8-carboxy-5-oxo-3-oxa-2,6,9-triazadecanedioic acid
(S)-11-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2,2-dimethyl-4,8-dioxo-3,6-dioxa-5,9-diazadodecan-12-oic acid
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-BETA-(TERT-BUTYLOXYCARBONYL-AMINOOXY-ACETYL)-L-2,3-DIAMINOPROPIONIC ACID
3-Oxa-2,6,9-triazadecanedioic acid, 8-carboxy-5-oxo-, 1-(1,1-dimethylethyl) 10-(9H-fluoren-9-ylmethyl) ester, (8S)-
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[[2-[(2-methylpropan-2-yl)oxycarbonylamino]oxyacetyl]amino]propanoic acid | [Molecular Formula]
C25H29N3O8 | [MDL Number]
MFCD02682868 | [MOL File]
600153-12-6.mol | [Molecular Weight]
499.51 |
| Hazard Information | Back Directory | [Chemical Properties]
White crystalline powder | [Uses]
peptide synthesis | [General Description]
An excellent derivative for the chemoselective ligation of unprotected peptides in aqueous media [1] via oxime formation. This derivative introduces a hydroxylamine functionality which can couple with aldehyde groups present in another peptide unit.
The product number for this product was previously 04-12-1185.
To obtain a certificate of analysis (CoA) of a lot that begins with the letter “A”, please select the option in the right hand menu “Request a COA for Lot#s starting with A”. | [reaction suitability]
reagent type: ligand |
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