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2-Ethoxycarbonylbenzeneboronic acid

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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
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
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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
pka
8.18±0.53(Predicted)
color 
White to Light yellow to Light orange
CAS DataBase Reference
380430-53-5(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36-37
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29319090
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2-Ethoxycarbonylbenzeneboronic acid Usage And Synthesis

Uses

suzuki reaction

Uses

Reactant 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

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