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Quinoline-4-boronic acid

CAT: 1139-371764-64-6-01Size: 10 gDry Ice: NoHazardous: No
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CAT#:1139-371764-64-6-01Size:10 g
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Description
Quinoline-4-boronic acid (CAS: 371764-64-6) is a high-purity nitrogen-containing heterocyclic boronic acid compound and critical fine chemical synthetic intermediate. It features a stable quinoline ring skeleton with active boronic acid functional groups, possessing excellent organic reaction activity and structural stability. Quinoline-4-boronic acid (CAS: 371764-64-6) has low side reaction rate and stable batch consistency, which is widely applicable to Suzuki coupling reactions, heterocyclic drug molecule derivation and high-end fine chemical customized synthesis in modern chemical and pharmaceutical industries.
Synonyms
4-Quinolineboronic acid, 4-Boronoquinoline, Quinolin-4-ylboronic acid, 4-Quinolylboronic acid
Applications
1. Industrial Suzuki Cross-Coupling Synthesis Application: Quinoline-4-boronic acid (CAS: 371764-64-6) serves as a core active monomer for industrial Suzuki cross-coupling reactions. The stable quinoline heterocyclic structure effectively improves reaction selectivity and conversion rate, reduces impurity generation in continuous industrial production, and is widely used for large-scale synthesis of quinoline derivative compounds. 2. Heterocyclic Pharmaceutical Intermediate Synthesis Application: Quinoline-4-boronic acid (CAS: 371764-64-6) is an essential precursor for the synthesis of quinoline-class targeted pharmaceutical intermediates. Its unique nitrogen heterocyclic structure can optimize the biological activity of drug molecules, supporting the R&D and industrial mass production of anti-tumor, anti-inflammatory and antibacterial drug intermediates. 3. High-end Fine Chemical Derivatization Application: Quinoline-4-boronic acid (CAS: 371764-64-6) acts as a key molecular building block for customized synthesis of high-value heterocyclic fine chemicals. The active boronic acid group supports precise structural grafting and modification, meeting the production demands of high-purity functional heterocyclic chemical products. 4. Laboratory Biochemical Synthetic Research Application: Quinoline-4-boronic acid (CAS: 371764-64-6) is a standard experimental reagent for exploring heterocyclic boronic acid synthesis mechanisms. It is widely used in laboratory organic synthesis experiments, new drug route development and biochemical structure-activity relationship research.
Purity
98%
Molecular Formula
C9H8BNO2
Molecular Weight
172.98
Shelf Life
2 years under proper storage
Appearance
White to Off-white Crystalline Powder
Grade
Research Grade, Pharmaceutical Intermediate Grade
Density
1.34±0.1 g/cm3
Melting Point
278-282 °C