2-Benzofuranylboronic acid
2-Benzofuranylboronic acid (CAS: 98437-24-2), with the empirical formula C8H7BO3 and a molecular weight of 161.95 g/mol, is a versatile organoboron compound. It is primarily utilised as a building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its structure facilitates the introduction of the benzofuranyl moiety into various molecular frameworks, making it valuable in the development of pharmaceuticals and advanced materials.
- IUPAC
- 2-Benzofuranboronic acid,Benzofuran-2-ylboronic acid
- Synonyms
- 2-Benzofuranboronic acidBenzofuran-2-ylboronic acid
Suzuki-Miyaura Cross-Coupling Reactions
2-Benzofuranylboronic acid serves as a key reagent in Suzuki-Miyaura cross-coupling reactions. This process enables the formation of carbon-carbon bonds by coupling organoboron compounds with organohalides, facilitating the synthesis of complex organic molecules.
Pharmaceutical Intermediate
This boronic acid derivative is employed in the synthesis of pharmacologically active compounds. The benzofuran core is present in several drug candidates, and this reagent allows for its efficient incorporation during medicinal chemistry research and development.
Materials Science
The compound finds application in the creation of novel materials, including organic semiconductors and optoelectronic devices. Its structural features can be exploited to tune the electronic and optical properties of advanced materials.
Heterocyclic Chemistry
As a heteroaryl boronic acid, it is a valuable tool for synthetic chemists working with heterocyclic scaffolds. It enables the construction and modification of complex heterocyclic systems prevalent in natural products and bioactive molecules.
| Molecular weight | 161.95 |
|---|---|
| Empirical formula | C8H7BO3 |
| Melting point | 114-116 °C(lit.) |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
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 is 2-Benzofuranylboronic acid used for?
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2-Benzofuranylboronic acid is primarily used as a building block in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions, and as an intermediate in the development of pharmaceuticals and advanced materials.
What are the CAS number and formula for 2-Benzofuranylboronic acid?
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The CAS number for 2-Benzofuranylboronic acid is 98437-24-2, and its empirical formula is C8H7BO3.
What grade and purity does Tech Serve Solutions supply?
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Tech Serve Solutions supplies 2-Benzofuranylboronic acid typically as a research or technical grade chemical. The precise assay is available on the Certificate of Analysis. TSS does not represent this product as USP, BP, EP, or other pharmacopoeial grades.
How should 2-Benzofuranylboronic acid be handled?
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Handling requires appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter is recommended. The substance has a WGK Germany classification of 3, indicating it is hazardous.
Is 2-Benzofuranylboronic acid a controlled substance?
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Based on the provided data, there is no indication that 2-Benzofuranylboronic acid is a controlled substance.
How is this product packed and shipped?
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Products are carefully packed according to international shipping regulations for chemicals. We export globally to research institutions and industries.
How can I request a quote or sample?
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To request a quote or a sample, please contact our sales team through the website or direct email, providing your specific requirements.
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