- 3-Quinolinylboronic acid
-
- $3.00 / 25KG
-
2025-10-13
- CAS:192182-56-2
- Min. Order: 0.1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
|
| | 4-Isoquinolineboronic acid Basic information |
| | 4-Isoquinolineboronic acid Chemical Properties |
| Melting point | 178°C | | Boiling point | 419.1±37.0 °C(Predicted) | | density | 1.28±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | form | solid | | pka | 4.61±0.30(Predicted) | | color | White to off-white | | InChI | 1S/C9H8BNO2/c12-10(13)9-6-11-5-7-3-1-2-4-8(7)9/h1-6,12-13H | | InChIKey | GDTOUTKTCGPAGY-UHFFFAOYSA-N | | SMILES | OB(O)c1cncc2ccccc12 | | CAS DataBase Reference | 192182-56-2(CAS DataBase Reference) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36/37/39 | | WGK Germany | WGK 3 | | HazardClass | IRRITANT | | HS Code | 29349990 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2
STOT SE 3 |
| Provider | Language |
|
ALFA
| English |
| | 4-Isoquinolineboronic acid Usage And Synthesis |
| Chemical Properties | Pink solid | | Uses | Reactant for:
- Preparation of selective steroid-11β-hydroxylase (CYP11B1) inhibitors for treatment of cortisol dependent diseases
- Preparation of tetrabutylammonium trifluoroborates
- Preparation of heteroaryl substituted tetrahydropyrroloijquinolinone derivatives as aldosterone synthase inhibitors
- Synthesis of aminoarylpyridazines as selective CB2 agonists for treatment of inflammatory pain
- Preparation of acyl substituted indoles via palladium-catalyzed domino coupling/carbonylation/Suzuki coupling of dibromoethenylanilines
- Synthesis of antagonists of bacterial quorum sensing
- Preparation of potassium heteroaryl trifluoroborates from boronic acids and their use as coupling partners with various aryl and heteroaryl halides in Suzuki-Miyaura cross-coupling reactions
| | General Description | May contain varying amounts of anhydride |
| | 4-Isoquinolineboronic acid Preparation Products And Raw materials |
|