| Identification | Back Directory | [Name]
TRANS-2-(4-METHOXYPHENYL)- | [CAS]
72316-18-8 | [Synonyms]
TRANS-2-(4-METHOXYPHENYL)-
(E)-(4-Methoxystyryl)boronic acid
[(E)-2-(4-Methoxyphenyl)ethenyl]boronic acid
(E)-2-(4-METHOXYPHENYL)ETHENYL-1-BORONIC ACID
trans-2-(4-Methoxyphenyl)vinylboronic acid >=95%
Boronic acid, B-[(1E)-2-(4-methoxyphenyl)ethenyl]- | [Molecular Formula]
C9H11BO3 | [MDL Number]
MFCD04039879 | [MOL File]
72316-18-8.mol | [Molecular Weight]
177.99 |
| Chemical Properties | Back Directory | [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) |
| Hazard Information | Back Directory | [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
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Energy Chemical
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http://www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
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021-61415566 800-8193336 |
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https://www.sigmaaldrich.cn |
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