5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID

5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID Basic information
Product Name:5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID
Synonyms:RARECHEM AH PB 0083;5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID;5-ISOPROPYL-2-METHOXYPHENYLBORONIC ACID;AKOS BRN-0316;5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID, 98+%;[2-Methoxy-5-(1-methylethyl)phenyl]boronic acid;(2-methoxy-5-propan-2-ylphenyl)boronic acid;2-Methoxy-5-isopropylphenylboronic acid
CAS:216393-63-4
MF:C10H15BO3
MW:194.04
EINECS:
Product Categories:Aryl;Boronic Acids;Boronic Acids and Derivatives;Aryl Boronic Acids;Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Disubstituted Aryl Boronic Acids;Organometallic Reagents
Mol File:216393-63-4.mol
5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID Structure
5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID Chemical Properties
Melting point 84-88 °C
Boiling point 350.0±52.0 °C(Predicted)
density 1.08±0.1 g/cm3(Predicted)
storage temp. 2-8°C
pka8.60±0.58(Predicted)
BRN 9193266
CAS DataBase Reference216393-63-4(CAS DataBase Reference)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 2931900090
MSDS Information
ProviderLanguage
ALFA English
5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID Usage And Synthesis
Uses5-Isopropyl-2-Methoxybenzeneboronic acid can be used as reactant involved in the synthesis of many biologically active molecules including Oxazolidinones for use as cholesteryl ester transfer protein inhibitors for atherosclerosis treatment; Selective quinazolinyl-phenol inhibitors of CHK1 as antitumor and radioprotectants; Biaryl-containing carbamates as CETP inhibitors and α -Sulfone hydroxamates as MMP inhibitors5Reactant involved in Suzuki-Miyaura cross coupling with 2-nitroarenediazonium tetrafluoroborate for synthesis of 2-nitrobiphenyls.
UsesReactant involved in the synthesis of many biologically active molecules including:
  • Oxazolidinones for use as cholesteryl ester transfer protein inhibitors for atherosclerosis treatment
  • Selective quinazolinyl-phenol inhibitors of CHK1 as antitumor and radioprotectants
  • Biaryl-containing carbamates as CETP inhibitors
  • α -Sulfone hydroxamates as MMP inhibitors

Reactant involved in Suzuki-Miyaura cross coupling with 2-nitroarenediazonium tetrafluoroborate for synthesis of 2-nitrobiphenyls
General DescriptionMay contain varying amounts of anhydride
5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID Preparation Products And Raw materials
3-ISOPROPYLPHENYLBORONIC ACID 5-TERT-BUTYL-2-METHOXYBENZENEBORONIC ACID 3-Tolylboronic acid 2-Methoxy-5-methylphenylboronic acid 2-Fluorophenylboronic acid 2-Hydroxyphenylboronic acid 3-ETHYLPHENYLBORONIC ACID 2-HYDROXY-5-METHYLPHENYLBORONIC ACID 5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID

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