Description

(4-(Methacryloyloxy)phenyl)boronic acid (CAS: 108305-42-6) is a high-purity boronic acid derivative featuring a methacryloyloxy functional group, making it a versatile building block for polymer chemistry and materials science. With the molecular formula C₁₀H₁₁BO₄, this compound is ideal for researchers developing advanced polymeric materials, sensors, and bio-conjugation reagents. Its IUPAC name, [4-(2-methylprop-2-enoyloxy)phenyl]boronic acid, reflects its reactive methacrylate and boronic acid moieties, enabling applications in controlled radical polymerization (e.g., RAFT, ATRP) and carbohydrate recognition. Packaged under inert conditions to ensure stability, this product is rigorously tested by HPLC and NMR to meet the highest standards for synthetic and biomedical research.

Properties

• CAS Number: 108305-42-6
• Complexity: 244
• IUPAC Name: [4-(2-methylprop-2-enoyloxy)phenyl]boronic acid
• InChI: InChI=1S/C10H11BO4/c1-7(2)10(12)15-9-5-3-8(4-6-9)11(13)14/h3-6,13-14H,1H2,2H3
• InChI Key: SWYSPVHUGOKMGH-UHFFFAOYSA-N
• Exact Mass: 206.0750390
• Molecular Formula: C10H11BO4
• Molecular Weight: 206.00
• SMILES: B(C1=CC=C(C=C1)OC(=O)C(=C)C)(O)O
• Topological: 66.8
• Monoisotopic Mass: 206.0750390
• Synonyms: (4-(Methacryloyloxy)phenyl)boronic acid, 108305-42-6, [4-(2-methylprop-2-enoyloxy)phenyl]boronic acid, 2-Propenoic acid,2-methyl-,4-boronophenyl ester, SCHEMBL2915973, MFCD33551457, (4-(Methacryloyloxy)phenyl)boronicacid, BS-45228, F72144

Application

This compound is widely used in polymer science as a functional monomer for synthesizing boronic acid-containing hydrogels and smart materials responsive to pH or sugars. It also serves as a key intermediate in biomedical applications, such as glucose-sensitive drug delivery systems and diagnostic sensors. Additionally, its boronic acid group enables covalent binding to diols, facilitating bioconjugation and surface modification for biosensors.

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