| TRANS-2-(4-(TRIFLUOROMETHYL)PHENYL)- Basic information |
| Product Name: | TRANS-2-(4-(TRIFLUOROMETHYL)PHENYL)- |
| Synonyms: | (E)-(4-(trifluoromethyl)styryl)boronic acid;TRANS-2-(4-(TRIFLUOROMETHYL)PHENYL)-;(4-(TrifluoroMethyl)styryl)boronic acid;trans-2-[4-(Trifluoromethyl)phenyl]vinylboronic acid >=95%;Boronic acid, B-[(1E)-2-[4-(trifluoromethyl)phenyl]ethenyl]-;{(E)-2-[4-(trifluoromethyl)phenyl]ethenyl}boronic acid;352525-91-8 |
| CAS: | 352525-91-8 |
| MF: | C9H8BF3O2 |
| MW: | 215.96 |
| EINECS: | |
| Product Categories: | Alkenyl;Boronic Acids;blocks;BoronicAcids;Boronic Acids and Derivatives |
| Mol File: | 352525-91-8.mol |
| TRANS-2-(4-(TRIFLUOROMETHYL)PHENYL)- Chemical Properties |
| Melting point | 204-210 °C(lit.) |
| Safety Information |
| WGK Germany | 3 |
| HS Code | 2931900090 |
| MSDS Information |
| TRANS-2-(4-(TRIFLUOROMETHYL)PHENYL)- Usage And Synthesis |
| Uses | trans-2-[4-(Trifluoromethyl)phenyl]vinylboronic Acid is used in preparation of novel chromane, isochromane, thiochromane, or tetrahydroquinoline derivatives as glucosylceramide synthase (GCS) inhibitors. |
| Uses | Reactant for:Microwave-assisted Suzuki-Miyaura cross-couplingCobalt-catalyzed coupling reactionsPreparation of vinylic MIDA boronatesSynthesis of C2-aryl pyrrolobenzodiazepine antitumor agentsSuzuki-Miyaura cross-coupling reaction |
| TRANS-2-(4-(TRIFLUOROMETHYL)PHENYL)- Preparation Products And Raw materials |
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