2-Bromoethyl acrylate, 94%, stab. with 900-1500ppm 4-methoxyphenol
2-Bromoethyl acrylate, 94%, stab. with 900-1500ppm 4-methoxyphenol
2-Bromoethyl acrylate, 94%, stab. with 900-1500ppm 4-methoxyphenol
2-Bromoethyl acrylate, 94%, stab. with 900-1500ppm 4-methoxyphenol
Thermo Scientific Chemicals

2-Bromoethyl acrylate, 94%, stab. with 900-1500ppm 4-methoxyphenol

CAS: 4823-47-6 | C5H7BrO2 | 179.013 g/mol
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Catalog number L12502.06
also known as L12502-06
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5 g
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Price (USD)
162.65
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Ends: 30-Jun-2026
191.00
Save 28.35 (15%)
Each
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Chemical Identifiers
CAS4823-47-6
IUPAC Name2-bromoethyl prop-2-enoate
Molecular FormulaC5H7BrO2
InChI KeyCDZAAIHWZYWBSS-UHFFFAOYSA-N
SMILESBrCCOC(=O)C=C
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SpecificationsSpecification SheetSpecification Sheet
Assay from Suppliers CofA≥92.5%
Comment900-1500 ppm 4-methoxyphenol as stabilizer
2-Bromoethyl acrylate is utilized in curable and reactive polymers due to the presence of reactive bromine. It is also used in the synthesis of other monomers.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Bromoethyl acrylate is utilized in curable and reactive polymers due to the presence of reactive bromine. It is also used in the synthesis of other monomers.

Solubility
Miscible with water.

Notes
Light and heat sensitive Incompatible with strong oxidizing agents, polymerizing agents and peroxides.
RUO – Research Use Only

General References:

  1. Mikulska, A.; Inoue, M.; Kuroda, K.; Iwanowska, A.; Yusa, S. I.; Nowakowska, M.; Szczubiałka, K. Polymeric/silicagel hybrid molecularly photoimprinted adsorbents for adenosine and its derivatives. Eur. Polym. J. 2014, 59, 230-238.
  2. Nagai, Y.; Tanami, T.; Abe, J.; Nagai, H.; Hamamizu, T.; Kominato, K.; Iida, K.; Nagasawa, K. Synthesis of 19-Nor-Vitamin DA-Ring Synthons via Ring-Closing Olefin Metathesis. Asian J. Org. Chem. 2014, 3 (9), 994-999.