TRANS-2-(4-METHOXYPHENYL)-

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
EINECS:
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
TRANS-2-(4-METHOXYPHENYL)- Structure
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
pka9.61±0.43(Predicted)
Safety Information
WGK Germany 3
HS Code 2931900090
MSDS Information
TRANS-2-(4-METHOXYPHENYL)- Usage And Synthesis
UsesReactant 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
UsesReactant 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)- Preparation Products And Raw materials
Preparation Products4-METHOXYCINNAMIC ACID
T-2-(3-(4-T-BU.-PHENYL)-2-ME-2-PROPENYL& TRANS-2-(4-METHYLPHENYL)VINYLBORONIC AC& TRANS-2-(4-FLUOROPHENYL)VINYLBORONIC ACID trans-2-(3-Fluorophenyl)vinylboronic acid RARECHEM AL BA 0105 RARECHEM AL BA 0108 RARECHEM AL BA 0251 RARECHEM AL BA 0228 RARECHEM AL BA 0106 TRANS-2-(4-METHOXYPHENYL)- RARECHEM AL BA 0107 2-(4-METHOXYPHENYL)-VINYLBORONIC ACID PINACOL ESTER RARECHEM AL BA 0253

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