2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride Basic information
- Product Name:
- 2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride
- Synonyms:
-
- 2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride
- 2-(2-(2-Aminoethoxy)ethoxy)acetic acid HCL
- 2-(2-(2-Aminoethoxy)
- AEEA-OH·HCl
- AEEA-OH
- CH2COOH-PEG2-NH2.HCl
- H-Ado-OH.HCl
- AEEA.HCl
- CAS:
- 134979-01-4
- MF:
- C6H14ClNO4
- MW:
- 199.63266
- Product Categories:
-
- peg
- 134979-01-4
- Mol File:
- 134979-01-4.mol
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride Chemical Properties
- storage temp.
- Inert atmosphere,Room Temperature
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride Usage And Synthesis
Uses
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride is an amino acid derivative salt reagent with an amino and carboxyl group at each end of its molecular structure, which can be used in the field of nucleic acid sequencing. It can also be used as a component for the synthesis of PNA oligoether conjugates. Single and double conjugation of 2-(2-(2-aminoethoxy)ethoxy)ethanol was obtained using carbonyldiimidazole. Multiple attachment of 2-(2-(2-(benzoyloxy)ethoxy)ethoxy)acetic acid building blocks to the N-terminus and β-amino groups of inserted diaminopropionic acid residues was achieved using a post-PNA assembly coupling procedure[1].
References
[1] ALICE GHIDINI. Synthesis of PNA oligoether conjugates.[J]. Molecules, 2014, 19 3: 3135-3148. DOI:10.3390/molecules19033135.
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2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride(134979-01-4)Related Product Information
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- 4-Aminophenylacetic acid
- Ethyl 2-(Chlorosulfonyl)acetate
- Glycine
- Iminodiacetic acid
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- 4-AMINOAZOBENZENE HYDROCHLORIDE
- D-Glucosamine hydrochloride
- Topotecan hydrochloride
- Phenylacetic acid
- Ethoxyacetic acid
- Acetic anhydride
- Ethoxy
- 2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride