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Boc-NH-PEG2-CH2COOH

Boc-NH-PEG2-CH2COOH Structure
CAS No.
108466-89-3
Chemical Name:
Boc-NH-PEG2-CH2COOH
Synonyms
2,2-DiMethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid;Boc-AEEA-OH;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;Boc-N-amido-PEG2-CH2CO2H;t-Boc-N-amido-PEG2-CH2CO2H;t-Boc-N-Amido-PEG2-CH2COOH
CBNumber:
CB02639228
Molecular Formula:
C11H21NO6
Molecular Weight:
263.29
MOL File:
108466-89-3.mol
MSDS File:
SDS
Modify Date:
2024/6/14 12:24:12

Boc-NH-PEG2-CH2COOH Properties

Boiling point 425.7±30.0 °C(Predicted)
Density 1.145±0.06 g/cm3(Predicted)
storage temp. -20°C
pka 3.40±0.10(Predicted)
form liquid
color 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

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HS Code  2918999090

Boc-NH-PEG2-CH2COOH price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 901577 t-Boc-N-amido-PEG2-CH2CO2H ≥95% 108466-89-3 50MG ₹2966.05 2022-06-14 Buy
Product number Packaging Price Buy
901577 50MG ₹2966.05 Buy

Boc-NH-PEG2-CH2COOH Chemical Properties,Uses,Production

Uses

t-Boc-N-amido-PEG2-CH2CO2H 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-PEG2-CH2CO2H 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.

Synthesis

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).

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Boc-N-amido-PEG2-CH2CO2H 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-DiMethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid 2-[2-[2-[(2-Methylpropan-2-yl)oxycarbonylaMino]ethoxy]ethoxy]acetic acid Boc-AEEA-OH 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 108466-89-3 137978-97-5 peg