(S)-(-)-2-Methyl-CBS-Oxazaborolidine; (S)-Me-CBS Catalyst CAS 112022-81-8 Factory
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CBS Catalysts
(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
| Chemical Name | (S)-(-)-2-Methyl-CBS-Oxazaborolidine (ca. 1mol/L in Toluene) |
| Synonyms | (S)-Me-CBS Catalyst; (S)-2-Methyl-CBS-Oxazaborolidine; (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine (ca. 1mol/L in Toluene) |
| CAS Number | 112022-81-8 |
| CAT Number | RF-CC106 |
| Stock Status | In Stock, Production Scale Up to Tons |
| Molecular Formula | C18H20BNO |
| Molecular Weight | 277.17 |
| Store Under Inert Gas | Store Under Inert Gas |
| Condition to Avoid | Moisture Sensitive |
| Melting Point | 85~95℃ (lit.) |
| Boiling Point | 111℃ |
| Density | 0.93 g/mL at 20℃ |
| Brand | Ruifu Chemical |
| Item | Specifications |
| Appearance | Colorless or Light Yellow Liquid |
| Identification | 1H NMR, IR |
| Concentration in Tol | 1mol/L |
| Assay | 28.5~31.5% |
| Test Standard | Enterprise Standard |
| Usage | CBS Catalysts |
Package: Bottle, Barrel, 25kg/Barrel, or according to customer's requirement.
Storage Condition: Store in sealed containers at cool and dry place; Protect from light, moisture and pest infestation.
Manufacturer Supply; High Quality and Competitive Price
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-Oxazaborolidine (CAS 112022-81-8), is an oxazaborolidine catalyst, a chiral catalyst used in chemical reactions, Usually used in the asymmetric reduction of prochiral ketones. Other applications include the enantioselective synthesis of α-hydroxy acids, α-amino acids, C2-symmetrical ferrocenyl diols, and propargyl alcohols.
(S)-(-)-2-Methyl-CBS-Oxazaborolidine (CAS 112022-81-8) Reaction
Convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures.
Asymmetric synthesis of α-chiral hydroxyalkylphosphines via a catalytic, enantioselective reduction of acylphosphines.
Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: Stereospecific formation of diarylalkanes and triarylmethanes.
Enantioselective reduction of prochiral ketones with NaBH4/Me2SO4/(S)-Me-CBS.
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