3-Vinylbenzoic acid, 96%, Thermo Scientific Chemicals
3-Vinylbenzoic acid, 96%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

3-Vinylbenzoic acid, 96%, Thermo Scientific Chemicals

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Quantity:
5 g
1 g
Catalog number H32556.06
also known as H32556-06
Price (USD)/ Each
180.65
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200.00 
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Quantity:
5 g
Request bulk or custom format
Price (USD)/ Each
180.65
Online exclusive
200.00 
Save 19.35 (10%)
Add to cart
3-Vinylbenzoic acid, 96%, Thermo Scientific Chemicals
Catalog numberH32556.06
Price (USD)/ Each
180.65
Online exclusive
200.00 
Save 19.35 (10%)
-
Add to cart
Chemical Identifiers
CAS28447-20-3
IUPAC Name3-ethenylbenzoic acid
Molecular FormulaC9H8O2
InChI KeyVWXZFDWVWMQRQR-UHFFFAOYSA-N
SMILESOC(=O)C1=CC=CC(C=C)=C1
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SpecificationsSpecification SheetSpecification Sheet
Assay (Silylated GC)>95.0%
Solution Test(10% w/v soln. in methanol) : Clear
Appearance (Color)White to pale yellow
FormPowder
Assay (Aqueous acid-base Titration)>95.0 to <105.0%
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Polymers were created by the imprinting of tri-O-acetyladenosine in acrylic polymer matrix with the use of methacrylic acid (MAA) or 3-vinylbenzoic acid (VBA) as a functional monomer and ethylene glycol dimethacrylate as a cross-linking agent. Nine active ester monomers based on 4-vinylbenzoic acid have been synthesized. Under free radical polymerization conditions these monomers could successfully be polymerized yielding reactive polymers

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
Polymers were created by the imprinting of tri-O-acetyladenosine in acrylic polymer matrix with the use of methacrylic acid (MAA) or 3-vinylbenzoic acid (VBA) as a functional monomer and ethylene glycol dimethacrylate as a cross-linking agent. Nine active ester monomers based on 4-vinylbenzoic acid have been synthesized. Under free radical polymerization conditions these monomers could successfully be polymerized yielding reactive polymers

Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, heat, light, ultraviolet radiations, free radical initiators.
RUO – Research Use Only

General References:

  1. Dr. Achillia Lakka,; Prof. Andreas Tsakalof. Molecular Imprinting of Tri-O-Acetyladenosine for the Synthetic Imitation of an ATP-Binding Cleft in Protein Kinases. ChemPlusChem. 2013, 78(8), 808-815.
  2. Xudong Geng,; Raphaël Geney,; Paula Pera,; Ralph J. Bernacki,; Iwao Ojim. Design and synthesis of de novo cytotoxic alkaloids through mimicking taxoid skeleton . Bioorganic & Medicinal Chemistry Letters. 2004, 14 (13),3491-3494.