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ChemicalBook--->CAS DataBase List--->106984-09-2

106984-09-2

106984-09-2 Structure

106984-09-2 Structure
IdentificationBack Directory
[Name]

N-BOC-AMINOEHTOXY-ETHOXY-ETHOXY-ETHANOL
[CAS]

106984-09-2
[Synonyms]

BocNH-PEG4-OH
N-Boc-PEG4-alcohol
t-boc-N-amido-PEG4-alcohol
N-BOC-AMINOEHTOXY-ETHOXY-ETHOXY-ETHANOL
N-Boc-aminoethoxy-ethoxy-ethoxy-ethanol
1-Boc-amino-3,6,9-trioxaundecanyl-11-ol
2-[2-(2-(2-Boc-aminoethoxy)ethoxy)ethoxy]ethanol
tert-Butyl 2-(2-(2-(2-hydroxyethoxy)-ethoxy)ethoxy)ethyl carbamate
(2-{2-[2-(2-Hydroxy-ethoxy)-ethoxy]-ethoxy}-ethyl)-carbamic Acid tert-Butyl Ester
[Molecular Formula]

C13H27NO6
[MDL Number]

MFCD07779195
[MOL File]

106984-09-2.mol
[Molecular Weight]

293.36
Chemical PropertiesBack Directory
[Appearance]

Yellow Oil
[Boiling point ]

414.0±35.0 °C(Predicted)
[density ]

1.078±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Oil
[pka]

12.23±0.46(Predicted)
[color ]

Clear Light Yellow
Questions And AnswerBack Directory
[Uses]

1-Boc-amino-3,6,9-trioxaundecanyl-11-ol is a compound useful in organic synthesis.
Hazard InformationBack Directory
[Chemical Properties]

Yellow Oil
[Description]

N-Boc-PEG4-alcohol is a PEG linker containing a hydroxyl group and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Safety DataBack Directory
[HS Code ]

2924190090
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