(S)-(-)-2-Methyl-CBS-Oxazaborolidine;(S)-Me-CBS Catalyst CAS 112022-81-8 Factory
Nomen chemicum | (S)-(-)-2-Methyl-CBS-Oxazaborolidinen (ca. 1mol/L in Toluene) |
Synonyma | (S)-Me-CBS Catalyst;(S)-2-Methyl-CBS-Oxazaborolidine;(S) -5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidines(ca. 1mol/L in Toluene) |
CAS Number | 112022-81-8 |
CATTUS Number | RF-CC106 |
Stock Status | In Stock, Productio Ascendite ad Tons |
Formulae hypotheticae | C18H20BNO |
M. Pondus | 277.17 |
Copia sub Inert Gas | Copia sub Inert Gas |
Conditio vitare | umorem Sensitivum |
Liquescens punctum | 85~95' (lit.) |
Ferveret | 111℃ |
Density | 0.93 g/mL in 20℃ |
Brand | Ruifu Chemical |
Item | Specifications |
Aspectus | Hyalina seu lux Yellow Liquid |
Lepidium sativum | 1H NMR, IR . |
Retrahitur in Tol | 1mol/L |
Assay | 28.5~ 31.5% |
Test Standard | Enterprise Standard |
Consuetudinem | CBS catalysts |
sarcina: Utrem, Ferocactus, 25kg/ Ferocactus, vel secundum exigentiam emptoris.
Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine, humore et pestis infestatione.
Manufacturer Supple;Qualitas et auctor pretium
CBS Catalyst
(S)-(-)-2-Methyl-CBS-Oxazaborolidine;(S)-Me-CBS Catalyst (ca. 1mol/L in Toluene);CAS: 112022-81-8
(R)-(+)-2-Methyl-CBS-Oxazaborolidine;(R)-Me-CBS Catalyst (ca. 1mol/L in Toluene);CAS: 112022-83-0
(S)-(-)-2-Methyl-CBS-Oxazaborolidinus (CAS 112022-81-8), catalysmus oxazaborolidus est, catalysta chiralis in reactionibus chemicis adhibita, Solet in reductione asymmetrica ketonum prochiralorum adhibita.Aliae applicationes includunt synthesim enantioselectivam ab acida hydroxy, amino acida, ferrocenyl diols C2-symmetricam, et alcoholum propargyl.
(S)-(-)-2-Methyl-CBS-Oxazaborolidini (CAS 112022-81-8) Reactio
Catalyst opportunus ad reductionem ketonum in ambientibus temperaturis enantiamelectivam boranam.
Synthesis asymmetrica α hydroxyalkylphosphinorum per catalyticam, enantioselectivam reductionem acylphosphinarum.
Nickel-catalysata crux iuncturae pivalatorum benzylicorum cum arylboroxinis: formatione stereospecifica diarylalkanorum et triarylmethanum.
Enantioselectivam reductionem prochiralorum ketonum cum NaBH4/Me2SO4/(S)-Me-CBS.