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Chemical Structure| 134978-97-5 Chemical Structure| 134978-97-5
Chemical Structure| 134978-97-5

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H2N-PEG2-CH2COOH is a 2-unit PEG derivative containing an amino group and a C2-carboxylic acid group. It is commonly used in bioconjugation and peptide synthesis applications.

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Product Details of H-AEEA-OH

CAS No. :134978-97-5
Formula : C6H13NO4
M.W : 163.17
SMILES Code : O=C(O)COCCOCCN
MDL No. :MFCD13185897
InChI Key :RUVRGYVESPRHSZ-UHFFFAOYSA-N
Pubchem ID :362706

Safety of H-AEEA-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of H-AEEA-OH

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 134978-97-5 ]

[ 134978-97-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 24424-99-5 ]
  • [ 134978-97-5 ]
  • [ 108466-89-3 ]
YieldReaction ConditionsOperation in experiment
62.1% With sodium carbonate; In 1,4-dioxane; water; at 20℃; for 12h; Step 3a: To a stirred solution of compound 1a (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 reaction was monitored by TLC. The reaction mass was partitioned between diethyl ether and water. Then aqueous layer was made acidic (pH=3) by 3N HCl solution and was extracted with DCM (2×200 mL). Organic layer was washed with water, brine, dried over Na2SO4 and evaporated under reduced pressure to yield 50 g of pure 3a (Yield: 62.1%). LCMS: 263.0 (M+H)+
62.1% With sodium carbonate; In 1,4-dioxane; water; at 20℃; for 12h; To a stirred solution of compound la (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)20 (9.98 mL, 45.7 mmol) were added and stirred at room temperature for 12 h. The progress ofreaction was monitored by TLC. The reaction mass was partitioned between diethyl ether and water. Then aqueous layer was made acidic (pH = 3) by 3N HC1 solution and was extracted with DCM (2 x 200 mL). Organic layer was washed with water, brine, dried over Na2504 and evaporated under reduced pressure to yield 50 g of pure 3a (Yield:62.1%). LCMS: 263.0 (M+H).
 

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