Bismut(III) Trifluoromethanesulfonate CAS 88189-03-1 Kemurnian >98.0% Bi 31.0~32.6%
Shanghai Ruifu Chemical Co., Ltd. is the leading manufacturer and supplier of Bismuth(III) Trifluoromethanesulfonate (CAS: 88189-03-1) with high quality. We can provide COA, worldwide delivery, small and bulk quantities available. Please contact: alvin@ruifuchem.com
Jeneng Kimia | Bismuth(III) Trifluoromethanesulfonate |
sinonim | Bi(OTf)3;Bismuth Tris (trifluoromethanesulfonate);Bismuth(III) Triflate;Bismuth Triflate;Trifluoromethanesulfonic Acid Bismuth Salt |
Nomer CAS | 88189-03-1 |
Nomer CAT | RF-PI2098 |
Status Simpenan | Ing Simpenan, Skala Produksi Nganti Ton |
Formula Molekul | C3BiF9O9S3 |
Bobot Molekul | 656.18 |
Titik Lebur | 300 ℃ |
Sensitivitas | Higroskopis |
Kelarutan | Larut ing Organik Acetonitrile, Dioxane, Dimetil Formamida lan Dimetil Sulfoksida |
Merk | Kimia Ruifu |
Item | Spesifikasi |
Penampilan | Bubuk Putih nganti Putih |
Kemurnian | >98.0% |
Bi (Complexiometric EDTA) | 31.0~32.6% |
Spektrum NMR Fluor | Conforms kanggo Struktur |
Proton NMR Spectrum | Conforms kanggo Struktur |
Spektrum Infrared | Conforms kanggo Struktur |
Test Standar | Standar Perusahaan |
Paket: Botol, tas Aluminium foil, 25kg / Karton Drum, utawa miturut kabutuhan pelanggan
Kondisi panyimpenan:Simpen ing wadhah sing disegel ing papan sing adhem lan garing;Nglindhungi saka cahya lan Kelembapan
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Bismuth(III) Trifluoromethanesulfonate (CAS: 88189-03-1) minangka asam Lewis kuat sing migunani ing sawetara reaksi katalitik.Katalis kanggo organiksintesis.Bismuth(III) Trifluoromethanesulfonate tumindak minangka katalis ing asilasi Friedel-Crafts lan cycloisomerization saka allene-enol eter.Iku tumindak minangka katalis substitusi langsung lan melu substitusi alkohol allylic, propargylic, lan benzilic karo sulfonamides, carboxamides lan carbamates.Salajengipun, uga digunakake ing reaksi aldol Mukaiyama.Bismut(III) trifluoromethanesulfonate bisa digunakake minangka katalis ing proses ing ngisor iki: deproteksi asetal;pemecahan turunan 2-tert-butoxy saka thiophenes lan furans;allylation saka asetals kanggo mbentuk eter homoallyl.
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