Boc-NH-PEG2-CH2COOH
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- CAS-Nr.
- 108466-89-3
- Englisch Name:
- Boc-NH-PEG2-CH2COOH
- Synonyma:
- Boc-AEEA-OH;2,2-DiMethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid;Boc-N-amido-PEG2-CH2CO2H;2-[2-[2-[(2-Methylpropan-2-yl)oxycarbonylaMino]ethoxy]ethoxy]acetic acid;Boc-O 2 Oc-OH;2-diMethyl-4-oxo-;BocNH-PEG2-CH2COOH;NHBoc-PEG2-CH2COOH;t-Boc-N-amido-PEG2-CH2CO2H;t-Boc-N-Amido-PEG2-CH2COOH
- CBNumber:
- CB02639228
- Summenformel:
- C11H21NO6
- Molgewicht:
- 263.29
- MOL-Datei:
- 108466-89-3.mol
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Boc-NH-PEG2-CH2COOH Eigenschaften
- Siedepunkt:
- 425.7±30.0 °C(Predicted)
- Dichte
- 1.145±0.06 g/cm3(Predicted)
- storage temp.
- -20°C
- pka
- 3.40±0.10(Predicted)
- Aggregatzustand
- liquid
- Farbe
- Yellow
- InChI
- InChI=1S/C11H21NO6/c1-11(2,3)18-10(15)12-4-5-16-6-7-17-8-9(13)14/h4-8H2,1-3H3,(H,12,15)(H,13,14)
- InChIKey
- OMBVJVWVXRNDSL-UHFFFAOYSA-N
- SMILES
- C(O)(=O)COCCOCCNC(=O)OC(C)(C)C
Boc-NH-PEG2-CH2COOH Chemische Eigenschaften,Einsatz,Produktion Methoden
Verwenden
t-Boc-
N-amido-PEG
2-CH
2CO
2H is a heterobifunctional, PEGylated crosslinker featuring a Boc-protected amine at one end and a carboxyl group at the other. The hydrophillic PEG linker facilitates solubility in biological applications. t-Boc-
N-amido-PEG
2-CH
2CO
2H 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.
Synthese
To a stirred solution of 2-(2-(2-Aminoethoxy)ethoxy)acetic acid (5.0 g, 30.6 mmol) in 1,4-Dioxane (50 mL), Sodium carbonate (8.12 g, 76.5 mmol, dissolved in 10 mL water) and (Boc)2O (9.98 mL, 45.7 mmol) were added and stirred at room temperature for 12 h. The progress of the reaction was monitored by TLC. The reaction mass was partitioned between diethyl ether and water. Then, the aqueous layer was made acidic (pH = 3) by 3N HC1 solution and was extracted with DCM (2 x 200 mL). The organic layer was washed with water, and brine, dried over Na2504 and evaporated under reduced pressure to yield 50 g of pure Boc-NH-PEG2-CH2COOH (Yield:62.1 per cent).
Boc-NH-PEG2-CH2COOH Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Boc-NH-PEG2-CH2COOH Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 209)Lieferanten
- t-boc-N-amido-PEG2-acetic acid
- 3,8,11-Trioxa-5-azatridecan-13-oic acid, 2,2-diMethyl-4-oxo-
- 8-tert-butyloxycarbonylaMino-3,6-dioxaoctanoic acid
- t-Boc-N-amido-PEG2-CH2CO2H
- BocNH-PEG2-CH2COOH
- T-BOC-NH-AMIDO-PEG2-CH2CO2H
- 2-[2-[2-(Boc-amino)ethoxy]ethoxy]acetic Acid
- 2-[2-(2-{[(tert-butoxy)carbonyl]amino}ethoxy)ethoxy]acetic acid
- 3,6,11-Trioxa-9-azatridecanoic acid, 12,12-dimethyl-10-oxo-
- 3,8,11-Trioxa-5-azatridecan-13-oic acid, 2,2-diMethyl-4-oxo- USP/EP/BP
- 11-Trioxa-5-azatridecan-13-oic acid
- 2-diMethyl-4-oxo-
- 2-[2-[2-[(2-Methylpropan-2-yl)oxycarbonylaMino]ethoxy]ethoxy]acetic acid
- NHBoc-PEG2-CH2COOH
- t-Boc-N-Amido-PEG2-CH2COOH
- N-Boc-8-amino-3,6-dioxaoctanoic acid
- Boc-O 2 Oc-OH
- 2-[2-(2-([(tert-butoxy)carbonylaminoJethoxy)ethoxylacetic acid
- 2,2-dimethyl-4,13-dioxo-3,8,11-trioxa-5-azatetradecan-14-oic acid
- Boc-NH-PEG2-CH2COOH/Boc-AEEA-OH
- t-Boc-N-amido-PEG2-CH2CO2H
- 2- [2- (tert butoxycarbonylamino) ethoxy] ethoxyacetic acid
- N-(tert-Butyloxycarbonyl)-8-amino-3,6-dioxaoctanoic acid
- 2,2-DiMethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid
- Boc-AEEA-OH
- Boc-N-amido-PEG2-CH2CO2H
- 108466-89-3
- 137978-97-5
- peg
