I-Isopropenylboronic Acid Pinacol Ester CAS 126726-62-3 Purity >99.0% (GC) Factory High Quality
Ukuhlinzeka Ngomkhiqizi Ngekhwalithi Ephezulu, Ukukhiqiza Kwezentengiso
Igama Lekhemikhali: Isopropenylboronic Acid Pinacol Ester
I-CAS: 126726-62-3
Igama Lekhemikhali | Isopropenylboronic Acid Pinacol Ester |
Omqondofana | 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl) -1,3,2-dioxaborolane;2-(1-Methylethenyl) -4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
Inombolo ye-CAS | 126726-62-3 |
Inombolo yeCAT | I-RF-PI1395 |
Isimo Sesitoko | Esitokweni, Isikali Sokukhiqiza Sifinyelela Kumathani |
I-Molecular Formula | I-C9H17BO2 |
Isisindo samangqamuzana | 168.04 |
Ibhrendi | I-Ruifu Chemical |
Into | Imininingwane |
Ukubukeka | Uketshezi Olungenambala Kuya Kuphuzi Okuphuzi |
Ukuhlanzeka / Indlela Yokuhlaziya | >99.0% (GC) |
Umswakama (KF) | ≤0.50% |
Ukungcola Okuphelele | <1.00% |
Izinga Lokuhlola | I-Enterprise Standard |
Ukusetshenziswa | Pharmaceutical Intermediates |
Iphakheji: Ibhodlela, 25kg/Umgqomo, noma ngokwezidingo zekhasimende.
Isimo Sesitoreji:Gcina ezitsheni ezivaliwe endaweni epholile neyomile;Vikela ekukhanyeni nakumswakama.
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I-Isopropenylboronic Acid Pinacol Ester (i-CAS: 126726-62-3) iyi-reagent ye-ester eguquguqukayo esetshenziselwa izinqubo zokuhlanganisa i-palladium-catalyzed Suzuki-Miyaura, i-inverse-electron-demand Diels-Alder reaction, i-Simmons-Smith cyclopropanation reaction, i-polyene cyclopropanation reaction ukusabela kwe-stereoelective aldol, ukusabela kwe-Grubbs cross-metathesis, ukusabela kwe-intramolecular Suzuki-Miyaura, i-Stereoselective cross-metathesis, i-dipole cycloaddition, i-iodosulfonylation, i-asymmetric conjugate add kanye ne-intramolecular hydroacylation kanye nokulungiswa kwe-kinase ehlukahlukene yokwelapha kanye ne-enzymatic.I-Isopropenylboronic Acid Pinacol Ester ingasetshenziswa njengendawo ephakathi ekuhlanganisweni kwezinhlobonhlobo zamakhompiyutha e-cyclic kanye ne-acyclic organic.Kuphinde kuboniswe ukuthi i-Al-Substituted Allyl/Croty yale nhlanganisela ingasetshenziselwa i-Diastereoand Enantioselective allylboration ye-aldehydes.