Description
2-Pyrrolylboronic acid (CAS No. 763120-43-0) is a high-purity boronic acid derivative with the molecular formula C4H6BNO2. This compound, also known by its IUPAC name 1H-pyrrol-2-ylboronic acid, is a versatile building block in organic synthesis and pharmaceutical research. Its pyrrole ring structure makes it particularly valuable in the development of heterocyclic compounds, Suzuki-Miyaura cross-coupling reactions, and as a precursor for functional materials.
Our 2-Pyrrolylboronic acid is rigorously tested for quality, ensuring optimal performance in sensitive applications. It is supplied as a white to off-white crystalline powder with high stability under recommended storage conditions. Researchers can rely on this reagent for consistent results in medicinal chemistry, catalysis, and materials science applications.
Key specifications include: ≥95% purity (HPLC), moisture content <0.5%, and heavy metals <10 ppm. The product is packaged under inert atmosphere to maintain stability and is available in quantities from grams to kilograms to meet both research and production needs.
Properties
- CAS Number: 763120-43-0
- Complexity: 78.4
- IUPAC Name: 1H-pyrrol-2-ylboronic acid
- InChI: InChI=1S/C4H6BNO2/c7-5(8)4-2-1-3-6-4/h1-3,6-8H
- InChI Key: WADSQZHEAXPENM-UHFFFAOYSA-N
- Exact Mass: 111.0491586
- Molecular Formula: C4H6BNO2
- Molecular Weight: 110.91
- SMILES: B(C1=CC=CN1)(O)O
- Topological: 56.3
- Monoisotopic Mass: 111.0491586
- Synonyms: 2-Pyrrolylboronic acid, 763120-43-0, DTXSID80400625, DTXCID80351481, 1H-pyrrol-2-ylboronic Acid, PYRROLE-2-BORONIC ACID, (1H-pyrrol-2-yl)boronic acid, 2-Pyrrolylboronicacid, Boronic acid, 1H-pyrrol-2-yl-, 2-pyrrolyl boronic acid, MFCD03095055, SCHEMBL488858, 1H-pyrrol-2-yl-2-boronic acid, WADSQZHEAXPENM-UHFFFAOYSA-N, AKOS006278865, AB13435, CS-35517, DB-010485, CS-0377022
Application
2-Pyrrolylboronic acid serves as a crucial intermediate in Suzuki-Miyaura cross-coupling reactions for creating biaryl compounds. It finds application in pharmaceutical research for developing novel drug candidates with pyrrole moieties. The compound is also used in materials science for synthesizing conjugated polymers and organic electronic materials. Its boronic acid functionality makes it valuable in sensor development and carbohydrate recognition systems.
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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


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