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CAS RN: 848821-58-9 | Product Number: D3843
(S)-(-)-α,α-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether
Purity: >98.0%(GC)(T)
Synonyms:
- (S)-(-)-2-[Diphenyl(trimethylsilyloxy)methyl]pyrrolidine
- α,α-Diphenyl-L-prolinol Trimethylsilyl Ether
- (S)-Hayashi-Jorgensen Catalyst
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days |
---|---|---|---|
1G |
$144.00
|
2 | Contact Us |
5G |
$463.00
|
5 | 4 |
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Product Number | D3843 |
Purity / Analysis Method | >98.0%(GC)(T) |
Molecular Formula / Molecular Weight | C__2__0H__2__7NOSi = 325.53 |
Physical State (20 deg.C) | Liquid |
Storage Temperature | Refrigerated (0-10°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Air Sensitive,Heat Sensitive |
CAS RN | 848821-58-9 |
Reaxys Registry Number | 10089429 |
PubChem Substance ID | 354334880 |
MDL Number | MFCD08690083 |
Specifications
Appearance | White to Yellow to Green clear liquid |
Purity(GC) | min. 98.0 % |
Purity(Nonaqueous Titration) | min. 98.0 % |
Specific rotation [a]20/D | -48.0 to -53.0 deg(C=1, CHCl3) |
Properties (reference)
Specific Gravity (20/20) | 1.04 |
Specific Rotation | -50° (C=1,CHCl3) |
Refractive Index | 1.55 |
Maximum Absorption Wavelength | 193 nm |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
H.S.code* | 2933.99-000 |
Application
Organocatalysts for Asymmetric Michael Additional Reactions
References
- 1) Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and Nitroalkenes
- 2) High-Yielding Synthesis of the Anti-Influenza Neuramidase Inhibitor (-)-Oseltamivir by Three “One-Pot” Operations
- 3) An Unexpected Organocatalytic Asymmetric Tandem Michael/Morita?Baylis?Hillman Reaction
- 4) Enantioselective Organocatalytic Michael/Aldol Sequence: Anticancer Natural Product (+)-trans-Dihydrolycoricidine
Application
Asymmetric Organocatalyst
Experimental procedure3): The β-ketoester 2 (0.2 mmol) is added to a solution of 3 (0.02 mmol), benzoic acid (0.02 mmol), and the aldehyde 1 (0.6 mmol) in toluene (0.2 mL). After complete consumption of 2, usually within 14–18 h, the crude product is directly charged on to silica gel and subjected to flash chromatography (hexane:Et2O) to afford 4.
References
- 1)Enantioselective Organocatalyzed α Sulfenylation of Aldehydes
- 2)Diphenylprolinol Silyl Ethers as Efficient Organocatalysts for the Asymmetric Michael Reaction of Aldehydes and Nitroalkenes
- 3)An Unexpected Organocatalytic Asymmetric Tandem Michael/Morita–Baylis–Hillman Reaction
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