Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of 8-Quinolineboronic Acid (CAS: 86-58-8) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. If you are interested in this product, please send detailed information includes CAS number, product name, quantity to us. Please contact: alvin@ruifuchem.com
Chemical Name |
8-Quinolineboronic Acid |
Synonyms |
Quinoline-8-Boronic Acid; 8-Quinolinylboronic Acid |
CAS Number |
86-58-8 |
CAT Number |
RF-PI1354 |
Stock Status |
In Stock, Production Capacity 25 Tons/Month |
Molecular Formula |
C9H8BNO2 |
Molecular Weight |
172.98 |
Brand |
Ruifu Chemical |
Item |
Specifications |
Appearance |
Light Yellow Crystal Powder |
Identification |
1H NMR spectrum corresponds to that of the standard preparation |
Identification |
The retention time of the major peak in the chromatogram corresponds to that in the chromatogram of standard preparation |
Purity / Analysis Method |
>98.0% (HPLC) |
Melting Point |
160.0~165.0℃ |
Moisture (K.F) |
≤0.20% |
Total Impurities |
<2.00% |
NMR |
Conforms to Structure |
Test Standard |
Enterprise Standard |
Usage |
Pharmaceutical Intermediates |
8-Quinolineboronic Acid (CAS: 86-58-8) HPLC Test Method |
Column: Eclipse plus C18, 250*4.6mm, 5um
Flow Rate: 1mL/min
Temp: Room Temp.
Mobile Phase : 75% ACN+0.1% TFA
Injection Volume: 20uL
Detection: 230nm |
Package: Bottle, Aluminium foil bag, 25kg/Cardboard Drum, or according to customer's requirement
Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture
8-Quinolineboronic Acid (CAS: 86-58-8) suzuki reaction. Reactant involved in: C-H and C-S bond activations; Synthesis of pyridazine via sequential amination / Suzuki coupling / alkylation reactions; Suzuki-Miyaura coupling reactions for synthesis of biaryl monophosphorus ligands, fused tricyclic oxa-quinolones, or substituted β-amino acids; Copper-catalyzed azidation with sodium azide; Studies of the affect of fluoride on the stability of boronic acids during click reactions.