(S)-(-)-2-Methyl-CBS-Oxazaborolidine;(S)-Me-CBS Catalyst CAS 112022-81-8 Factory

Description:

(S)-(-)-2-Methyl-CBS-Oxazaborolidinen (ca. 1mol/L in Toluene)

Synonyma:(S)-Me-CBS Catalyst (ca. 1mol/L in Toluene)

CAS: 112022-81-8

Aspectus: hyalina seu lux Yellow liquida

Retrahitur: 1.0Mol

Pertentare: 28.5~ 31.5%


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Descriptio:

Chemical Properties:

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

Specifications:

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 & Repono:

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.

commoda:

1

FAQ:

2

Applicatio:

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.

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