Competitive Price for 2-Deoxyadenosine-5-monophosphate Free Acid - 4-Pyridylboronic Acid CAS 1692-15-5 Purity ≥99.5% (HPLC) Factory Hot Sale – Ruifu
Competitive Price for 2-Deoxyadenosine-5-monophosphate Free Acid - 4-Pyridylboronic Acid CAS 1692-15-5 Purity ≥99.5% (HPLC) Factory Hot Sale – Ruifu Detail:
Manufacturer Supply, High Purity, Commercial Production
Chemical Name: 4-Pyridylboronic Acid
CAS: 1692-15-5
Chemical Name | 4-Pyridylboronic Acid |
Synonyms | Pyridine-4-Boronic Acid |
CAS Number | 1692-15-5 |
CAT Number | RF-PI571 |
Stock Status | In Stock, Production Scale Up to Tons |
Molecular Formula | C5H6BNO2 |
Molecular Weight | 122.92 |
Solubility | Insoluble in Water |
Melting Point | >300℃ (lit.) |
Brand | Ruifu Chemical |
Item | Specifications |
Appearance | White Powder |
Moisture (K.F) | ≤0.50% |
Purity / Analysis Method | ≥99.0% (HPLC) |
Single Impurity | ≤0.50% |
Total Impurities | ≤1.0% |
Test Standard | Enterprise Standard |
Usage | Pharmaceutical Intermediates |
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.
4-Pyridylboronic Acid (CAS: 1692-15-5) can be used as a candidate for Suzuki-Miyaura coupling reaction. Especially, as a N-containing building blocks, pyridine-4-boronic acid was employed to construct some heterocyclic compounds with superior biological activities. 4-Pyridylboronic Acid is a kind of boronic acid derivative. It is useful building blocks in crystal engineering. It can also be used as a catalyst to act as a dehydrative condensation agent to synthesize amides using carboxylic acid and amines as raw materials. Its derivative, polystyrene-bound 4-pyridineboronic acid, is a useful catalyst for amidation reaction and esterification of alpha-hydrocarboxylic acids.
Reagent used for: Palladium-catalyzed Suzuki-Miyaura coupling reactions; Ligand-free palladium-catalyzed Suzuki coupling reaction under microwave irradation; Reagent used in: Preparation of HIV-1 protease inhibitors; Potential cancer threapeutics, such as PDK1 and protein kinase CK2 inhibitors.
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