Identification | More | [Name]
4-Isoquinolineboronic acid | [CAS]
192182-56-2 | [Synonyms]
4-ISOQUINOLINEBORONIC ACID 4-ISOQUINOLINYLBORONI ACID 5-ISOQUINOLINEBORONIC ACID AKOS BRN-0121 AKOS BRN-0458 CHEMBRDG-BB 4002849 ISOQUINOLIN-4-YLBORONIC ACID ISOQUINOLIN-5-YLBORONIC ACID ISOQUINOLINE-4-BORONIC ACID ISOQUINOLINE-5-BORONIC ACID RARECHEM AK VD 0025 RARECHEM AK VD 0026 ISOQUINOLYL-4-YL-BORONIC ACID Isoquinoline-4-boronic acid, 2,2-dimethylpropane-1,3-diol cyclic ester 4-Isoquinolinylboronic acid | [Molecular Formula]
C9H8BNO2 | [MDL Number]
MFCD03839356 | [Molecular Weight]
172.98 | [MOL File]
192182-56-2.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29349990 |
Hazard Information | Back Directory | [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 |
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