ChemicalBook--->CAS DataBase List--->1286281-32-0

1286281-32-0

1286281-32-0 Structure

1286281-32-0 Structure
IdentificationBack Directory
[Name]

H2N-PEG6-tBu
[CAS]

1286281-32-0
[Synonyms]

H2N-PEG6-tBu
NH2-PEG6-Boc
1286281-32-0
Amino-PEG6-COOtBu
H2N-PEG6-CH2CH2COOtBu
NH2-PEG6-CH2CH2COOtBu
Amino-PEG6-t-butyl ester
Amino-PEG7-t-butyl ester
Amino-dPEG??-t-butyl ester
H2N-PEG6-CH2CH2-t-butylester
t-Butyl 3-Amino(peg6)propionate
Amino-PEG6-t-butylester,H2N-PEG6-t-butyl ester
tert-Butyl 1-amino-3,6,9,12,15,18-hexaoxahenicosan-21-oate
4,7,10,13,16,19-Hexaoxaheneicosanoic acid, 21-amino-, 1,1-dimethylethyl ester
[Molecular Formula]

C19H39NO8
[MDL Number]

MFCD13184944
[MOL File]

1286281-32-0.mol
[Molecular Weight]

409.51
Chemical PropertiesBack Directory
[Boiling point ]

475.9±40.0 °C(Predicted)
[density ]

1.056±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[pka]

8.74±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2942000090
Hazard InformationBack Directory
[Description]

Amino-PEG6-t-butyl ester is a PEG reagent containing an amino NH2 group with a t-butyl protected carboxyl group (Boc). The hydrophilic PEG spacer increases solubility in aqueous media. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
[Uses]

This heterobifunctional, PEGylated crosslinker features an amino group at one end and t-butyl-protected carboxyl group at the other, which can be deprotected with acidic conditions. The hydrophillic PEG linker facilitates solubility in biological applications. Amino-PEG6-t-butyl ester can be used for bioconjugation or as a building block for synthesis of small molecules, conjugates of small molecules and/or biomolecules, or other tool compounds for chemical biology and medicinal chemistry that require ligation. Examples of applications include its synthetic incorporation into antibody-drug conjugates or proteolysis-targeting chimeras (PROTAC? molecules) for targeted protein degradation.
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