2-Ethoxycarbonylbenzeneboronic acid

2-Ethoxycarbonylbenzeneboronic acid
  • CAS No.:380430-53-5
Other grades of this product :
2-Ethoxycarbonylbenzeneboronic acid Basic information
Product Name:2-Ethoxycarbonylbenzeneboronic acid
Synonyms:ETHYL 2-BORONOBENZOATE;2-CARBETHOXY-PHENYL-BORONIC ACID;2-ETHOXYCARBONYLBENZENEBORONIC ACID;2-ETHOXYCARBONYLPHENYLBORONIC ACID;O-ETHOXYCARBONYLPHENYLBORONIC ACID;Ethyl 2-Boronobenzoat;2-ETHOXYCARNONYLPHENYLBORNIC ACID;Benzoic acid, 2-borono-, 1-ethyl ester (9CI)
CAS:380430-53-5
MF:C9H11BO4
MW:193.99
EINECS:
Product Categories:Boronate Ester;Boronic Acid;Aryl;Boronic Acids;Boronic Acids and Derivatives;Potassium Trifluoroborate;CARBOXYLICESTER;BORONICACID;blocks;BoronicAcids;Carboxes;Substituted Boronic Acids;Boronic acids
Mol File:380430-53-5.mol
2-Ethoxycarbonylbenzeneboronic acid Chemical Properties
Melting point 137 °C
Boiling point 367.5±44.0 °C(Predicted)
density 1.21±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Methanol
form powder or crystals
pka8.18±0.53(Predicted)
color White to Light yellow to Light orange
CAS DataBase Reference380430-53-5(CAS DataBase Reference)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36-37
WGK Germany 3
HazardClass IRRITANT
HS Code 29319090
MSDS Information
2-Ethoxycarbonylbenzeneboronic acid Usage And Synthesis
Usessuzuki reaction
UsesReactant for:
  • Synthesis of embelin derivatives via Suzuki-Miyaura reaction, cross metathesis and Wittig olefination
  • Asymmetric cyclopropanation of alkenes with di-Me diazomalonate catalyzed by chiral diene-rhodium complexes
  • Preparation of phenylalanines as selective AMPA- and kainate receptor ligands
  • Preparation of aryl pyrazinones via microwave-assisted palladium-catalyzed arylation of resin supported pyrazinones under simultaneous cooling condition
  • Regioselective preparation of (aryl)hydroxyquinolines via Suzuki-Miyaura cross-coupling with chloro(tosyloxy)quinoline under anhydrous conditions followed by nucleophilic deprotection of the tosyl group
2-Ethoxycarbonylbenzeneboronic acid Preparation Products And Raw materials

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