| Company Name: |
Energy Chemical |
| Tel: |
400-0056266 |
| Email: |
sales8178@energy-chemical.com |
|
| | trans-2-(4-Methoxyphenyl)- Basic information |
| | 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) | | Appearance | Light yellow to brown Solid | | InChI | 1S/C9H11BO3/c1-13-9-4-2-8(3-5-9)6-7-10(11)12/h2-7,11-12H,1H3/b7-6+ | | InChIKey | LGSBCAPDUJYMOQ-VOTSOKGWSA-N | | SMILES | COc1ccc(\C=C\B(O)O)cc1 |
| WGK Germany | 3 | | HS Code | 2931900090 | | Storage Class | 11 - Combustible Solids |
| | 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
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| | trans-2-(4-Methoxyphenyl)- Preparation Products And Raw materials |
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