ChemicalBook Product Catalog Chemical Reagents Organic reagents Boric acid 4-Isoquinolineboronic acid

4-Isoquinolineboronic acid

4-Isoquinolineboronic acid Basic information
Product Name:4-Isoquinolineboronic acid
Synonyms:CHEMBRDG-BB 4002849;ISOQUINOLIN-5-YLBORONIC ACID;ISOQUINOLIN-4-YLBORONIC ACID;ISOQUINOLINE-4-BORONIC ACID;4-ISOQUINOLINEBORONIC ACID;4-ISOQUINOLINYLBORONI ACID;AKOS BRN-0121;AKOS BRN-0458
CAS:192182-56-2
MF:C9H8BNO2
MW:172.98
EINECS:
Product Categories:Boric Acid| Boric Acid Ester| Potassium Trifluoroborate;Boronic Acids & Esters;Quinolines, Isoquinolines & Quinoxalines;Quinoline&Isoquinoline;Boronic acid;Isoquinoline;Organoborons;Boronic Acids & Esters;Quinolines, Isoquinolines & Quinoxalines;blocks;BoronicAcids;Quinolines
Mol File:192182-56-2.mol
4-Isoquinolineboronic acid Structure
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
pka4.61±0.30(Predicted)
color White to off-white
CAS DataBase Reference192182-56-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39
HazardClass IRRITANT
HS Code 29349990
MSDS Information
ProviderLanguage
ALFA English
4-Isoquinolineboronic acid Usage And Synthesis
Chemical PropertiesPink solid
UsesReactant 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 DescriptionMay contain varying amounts of anhydride
4-Isoquinolineboronic acid Preparation Products And Raw materials
Raw materialsDiethyl ether-->Tetrahydrofuran-->Government regulation-->n-Butyllithium-->Nitrogen-->Hydrogen bromide-->Triisopropyl borate-->Isoquinoline-->4-Bromoisoquinoline
Preparation Products4-NITROISOQUINOLINE
tert-Butyl[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin -2-yl]carbamate Isoquinolin-3-ylMethanaMine hydrochloride 3-isoquinolinecarboxaldehyde ISOQUINOLINE-1-CARBALDEHYDE 1-ISOQUINOLINEMETHANOL 3-Isoquinolinol(9CI) ISOQUINOLINE-1-CARBOXYLIC ACID METHYL ESTER ISOQUINOLIN-6-YLMETHANOL 6-isoquinolinecarboxylic acid C-ISOQUINOLIN-1-YL-METHYLAMINE DIHYDROCHLORIDE 7-Isoquinolinecarbonitrile(9CI) 7-isoquinolinecarboxylic acid 3-METHYL-1-BUTYLBORONIC ACID 5-ISOQUINOLINEBORONIC ACID,5-ISOQUINOLINEBORONIC ACID, HCL 8-Isoquinolineboronic acid QUINOLINE-4-BORONIC ACID 1-CHLORO-4-ISOQUINOLINYL BORONIC ACID 1-ISOQUINOLINEBORONIC ACID
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