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TRANS-2-(4-METHOXYPHENYL)-

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TRANS-2-(4-METHOXYPHENYL)- Basic information

Product Name:
TRANS-2-(4-METHOXYPHENYL)-
Synonyms:
  • TRANS-2-(4-METHOXYPHENYL)-
  • (E)-2-(4-METHOXYPHENYL)ETHENYL-1-BORONIC ACID
  • [(E)-2-(4-Methoxyphenyl)ethenyl]boronic acid
  • (E)-(4-Methoxystyryl)boronic acid
  • trans-2-(4-Methoxyphenyl)vinylboronic acid >=95%
  • Boronic acid, B-[(1E)-2-(4-methoxyphenyl)ethenyl]-
CAS:
72316-18-8
MF:
C9H11BO3
MW:
177.99
Product Categories:
  • Alkenyl Boronic Acids
  • Boronic Acids
  • Alkenyl
  • Boronic Acids and Derivatives
  • Chemical Synthesis
  • Organometallic Reagents
  • blocks
  • BoronicAcids
  • Boronic Acids
  • Boronic Acids and Derivatives
Mol File:
72316-18-8.mol
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TRANS-2-(4-METHOXYPHENYL)- Chemical Properties

Melting point:
140-144 °C(lit.)
Boiling point:
373.1±44.0 °C(Predicted)
Density 
1.149±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
9.61±0.43(Predicted)
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Safety Information

WGK Germany 
3
HS Code 
2931900090
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TRANS-2-(4-METHOXYPHENYL)- Usage And Synthesis

Uses

Reactant involved in:• ;Enantioselective conjugate addition reactions with indole-appended enones1• ;Liebeskind-Srogl cross-coupling reactions2• ;Petasis asymmetric dihydroxylation for synthesis of (dihydroxy)homotyrosines3• ;Copper-catalyzed trifluoromethylation4• ;Asymmetric Michael addition with hydroxycinnamaldehydes5• ;Cobalt-catalyzed coupling for synthesis of phenylbutenylheteroarenes6

Uses

Reactant involved in:

  • Enantioselective conjugate addition reactions with indole-appended enones
  • Liebeskind-Srogl cross-coupling reactions
  • Petasis asymmetric dihydroxylation for synthesis of (dihydroxy)homotyrosines
  • Copper-catalyzed trifluoromethylation
  • Asymmetric Michael addition with hydroxycinnamaldehydes
  • Cobalt-catalyzed coupling for synthesis of phenylbutenylheteroarenes

TRANS-2-(4-METHOXYPHENYL)-Supplier

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