Description
Quinolin-5-ylboronic acid (CAS No. 355386-94-6) is a high-purity boronic acid derivative with the molecular formula C9H8BNO2. This compound is a valuable building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, due to its reactive boronic acid functional group. The quinoline backbone provides enhanced stability and electronic properties, making it ideal for pharmaceutical and materials science research. Our product is rigorously tested to ensure ≥95% purity (HPLC) and is supplied as a white to off-white crystalline powder. Suitable for use in medicinal chemistry, catalysis, and polymer synthesis, it is packaged under inert conditions to guarantee stability and longevity.
Synonyms: Quinoline-5-boronic acid, 5-Quinolineboronic acid
Storage: Store in a cool, dry place at 2-8°C under inert atmosphere. Protect from moisture and light.
Properties
- CAS Number: 355386-94-6
- Complexity: 177
- IUPAC Name: 5-quinolylboronic acid
- InChI: InChI=1S/C9H8BNO2/c12-10(13)8-4-1-5-9-7(8)3-2-6-11-9/h1-6,12-13H
- InChI Key: NWIJBOCPTGHGIK-UHFFFAOYSA-N
- Exact Mass: 173.0648087
- Molecular Formula: C9H8BNO2
- Molecular Weight: 172.98
- SMILES: B(C1=C2C=CC=NC2=CC=C1)(O)O
- Topological: 53.4
- Monoisotopic Mass: 173.0648087
- Synonyms: Quinolin-5-ylboronic Acid, 670-357-0, Quinoline-5-boronic acid, 355386-94-6, 5-Quinolineboronic acid, 5-quinolinylboronic acid, quinolin-5-yl-5-boronic acid, MFCD03095058, (quinolin-5-yl)boronic acid, BORONIC ACID, 5-QUINOLINYL-, Quinolin-5-ylboronicAcid, SCHEMBL20346, DTXSID90408935, NWIJBOCPTGHGIK-UHFFFAOYSA-N, BCP23481, Quinoline-5-boronic acid, AldrichCPR, AKOS003237497, AB13438, AC-6959, CS-W003017, HY-W003017, PS-9467, SY003941, DB-024746, Q0087, EN300-212551, Quinoline-5-boronic Acid(contains varying amounts of Anhydride)
Application
Quinolin-5-ylboronic acid is widely used in palladium-catalyzed cross-coupling reactions to form biaryl compounds, a key step in drug discovery and material science. It serves as a critical intermediate in the synthesis of quinoline-based pharmaceuticals, including kinase inhibitors and antimicrobial agents. Researchers also employ it in the development of fluorescent probes and organic electronic materials due to its conjugated aromatic system.
Safety and Hazards
GHS Hazard Statements
- H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
- H335 (97.8%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statements
- P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501
Hazard Classes and Categories
- Skin Irrit. 2 (100%)
- Eye Irrit. 2 (100%)
- STOT SE 3 (97.8%)
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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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