707929
4-Isoquinolineboronic acid
Synonym(s):
Isoquinolin-4-ylboronic acid, Isoquinoline-4-boronic acid
About This Item
Recommended Products
form
solid
Quality Level
mp
230-234 °C
storage temp.
2-8°C
SMILES string
OB(O)c1cncc2ccccc12
InChI
1S/C9H8BNO2/c12-10(13)9-6-11-5-7-3-1-2-4-8(7)9/h1-6,12-13H
InChI key
GDTOUTKTCGPAGY-UHFFFAOYSA-N
General description
Application
- 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
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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