3-Vinylphenylboronic acid
3-Vinylphenylboronic acid (CAS: 15016-43-0, Formula: C8H9BO2, MW: 147.97) is a versatile organoboron compound. It serves as a key reactant in Suzuki-Miyaura cross-coupling reactions and is employed in the synthesis of various organic molecules. Its applications extend to molecular imprinting and the generation of acyl anion equivalents, making it a valuable reagent in chemical synthesis.
- IUPAC
- (3-Ethenylphenyl)boronic acid,m-Vinylbenzeneboronic acid
Suzuki-Miyaura Cross-Coupling
This compound is a crucial reactant in Suzuki-Miyaura reactions, enabling the formation of carbon-carbon bonds. It facilitates the synthesis of biaryl compounds and other complex organic structures.
Molecular Imprinting
3-Vinylphenylboronic acid is utilised in the molecular imprinting process for specific analytes like fructose and pinacol. This technique allows for the creation of selective binding sites.
Organic Synthesis Reagent
It participates in reactions such as Chen-Lam-Evans arylation for generating arylmercapturic acids and in three-component couplings to yield diarylketones. It also acts as a precursor for acyl anion equivalents.
| Molecular weight | 147.97 |
|---|---|
| Empirical formula | C8H9BO2 |
| Storage temperature | 2-8°C |
| Application | Reactant involved in:• Suzuki-Miyaura reactions1• Molecular imprinting of fructose and pinacol2• Synthesis of arylmercapturic acids via Chen-Lam-Evans arylation3• Three-component cross-coupling yeilding diarylketones4• Generation of acyl anion equivalents5 |
| Melting point | 141-147 °C |
Hazard statements
- H301Toxic if swallowed
Precautionary statements
- P301IF SWALLOWED
| Protective equipment | dust mask type N95 (US), Eyeshields, Faceshields, Gloves |
|---|---|
| Transport (UN / ADR) | UN 2811 6.1 / PGIII |
| Water hazard class (WGK, DE) | 3 |
| Hazard codes (EU) | Xn |
| Risk statements (R) | 22 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What are the primary applications of 3-Vinylphenylboronic acid?
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3-Vinylphenylboronic acid is used as a reactant in Suzuki-Miyaura reactions, in molecular imprinting of fructose and pinacol, in the synthesis of arylmercapturic acids via Chen-Lam-Evans arylation, in three-component cross-couplings yielding diarylketones, and for generating acyl anion equivalents.
What is the CAS number and molecular formula for 3-Vinylphenylboronic acid?
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The CAS number is 15016-43-0, and the molecular formula is C8H9BO2.
What grade and purity does Tech Serve Solutions supply for 3-Vinylphenylboronic acid?
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Tech Serve Solutions supplies 3-Vinylphenylboronic acid as a research-grade chemical. The assay is not specified beyond 'technical/research grade'; TSS does not represent this product as USP, BP, or EP grade.
How should 3-Vinylphenylboronic acid be handled safely?
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3-Vinylphenylboronic acid is classified as Danger (GHS06) with hazard statement H301 (Toxic if swallowed). Handle with appropriate personal protective equipment, including a dust mask (type N95 or equivalent), eyeshields, face shields, and gloves. Follow precautionary statement P301 + P310 (If swallowed: Immediately call a poison center or doctor).
Is 3-Vinylphenylboronic acid a controlled substance?
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The provided data does not indicate that 3-Vinylphenylboronic acid is a controlled substance.
How is 3-Vinylphenylboronic acid shipped and exported?
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3-Vinylphenylboronic acid is shipped and exported according to UN 2811, Hazard Class 6.1, Packing Group III regulations. Storage is recommended at 2-8°C.
How can I request a quote or sample of 3-Vinylphenylboronic acid?
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To request a quote or sample, please contact our sales department via the website or direct inquiry channels.
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