ChemicalBook--->CAS DataBase List--->600153-12-6

600153-12-6

600153-12-6 Structure

600153-12-6 Structure
IdentificationBack 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
Chemical PropertiesBack Directory
[density ]

1.304±0.06 g/cm3(Predicted)
[storage temp. ]

Store below +30°C.
[pka]

3.41±0.10(Predicted)
Safety DataBack Directory
[HS Code ]

29225090
Hazard InformationBack Directory
[Chemical Properties]

White crystalline powder
[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.

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