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5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID

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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
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
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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
pka
8.60±0.58(Predicted)
BRN 
9193266
CAS DataBase Reference
216393-63-4(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2931900090

MSDS

  • Language:English Provider:ALFA
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5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACID Usage And Synthesis

Uses

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
  • α -Sulfone hydroxamates as MMP inhibitors

Reactant involved in Suzuki-Miyaura cross coupling with 2-nitroarenediazonium tetrafluoroborate for synthesis of 2-nitrobiphenyls

Uses

5-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.

General Description

May contain varying amounts of anhydride

5-ISOPROPYL-2-METHOXYBENZENEBORONIC ACIDSupplier

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