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1020112-73-5

1020112-73-5 Structure

1020112-73-5 Structure
IdentificationBack Directory
[Name]

2-Amino-1,3-bis(carboxylethoxy)propane HCl salt
[CAS]

1020112-73-5
[Synonyms]

2-Amino-1,3-bis(carboxylethoxy)propane
2-Amino-1,3-bis(carboxylethoxy)propane HCl salt
Propanoic acid, 3,3'-[(2-amino-1,3-propanediyl)bis(oxy)]bis-
3,3'-[(2-Aminopropane-1,3-diyl)bis(oxy)]dipropanoic Acid Hydrochloride
[Molecular Formula]

C9H17NO6
[MDL Number]

MFCD31692207
[MOL File]

1020112-73-5.mol
[Molecular Weight]

235.23
Chemical PropertiesBack Directory
[Boiling point ]

478.1±45.0 °C(Predicted)
[density ]

1.284±0.06 g/cm3(Predicted)
[pka]

3.94±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Description]

2-Amino-1,3-bis(carboxylethoxy)propane is a chemical reagent containing an amino group with two terminal carboxylic acids. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The terminal carboxylic acids can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
[Uses]

2-Amino-13-bis(carboxylethoxy)propane is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1].
[IC 50]

PEGs
[References]

[1] An S, et al. Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs. EBioMedicine. 2018 Oct;36:553-562 DOI:10.1016/j.ebiom.2018.09.005
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