Ethanol, 2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]-
Ethanol, 2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]- Basic information
- Product Name:
- Ethanol, 2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]-
- Synonyms:
-
- Ethanol, 2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]-
- 2-[2-[2-(2-BroMoethoxy)ethoxy]ethoxy]-ethanol
- Bromo-PEG4
- Bromo-PEG4-alcohol
- Br-PEG4-OH
- Br-PEG4-OH, Bromo-PEG4-alcohol
- 2-{2-[2-(2-bromoethoxy)ethoxy]ethoxy}ethan-1-ol
- HO-(CH2CH2O)4-Br
- CAS:
- 85141-94-2
- MF:
- C8H17BrO4
- MW:
- 257.12
- Mol File:
- 85141-94-2.mol
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Ethanol, 2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]- Chemical Properties
- Boiling point:
- 321.7±27.0 °C(Predicted)
- Density
- 1.350±0.06 g/cm3(Predicted)
- storage temp.
- Storage temp. 2-8°C
- pka
- 14.36±0.10(Predicted)
- form
- Liquid
- color
- Colorless to light yellow
- InChI
- InChI=1S/C8H17BrO4/c9-1-3-11-5-7-13-8-6-12-4-2-10/h10H,1-8H2
- InChIKey
- CERQCRALBKUCTF-UHFFFAOYSA-N
- SMILES
- C(O)COCCOCCOCCBr
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Ethanol, 2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]- Usage And Synthesis
Description
Bromo-PEG4-alcohol is a PEG linker containing a bromide group and a terminal hydroxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
Uses
Br-PEG4-OH 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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