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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:
1G
$144.00
2   Contact Us
5G
$463.00
5   4  

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* The storage conditions are subject to change without notice.


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 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
*This code is applied to the products when TCI exports from Japan and not for import in your country.
Application
Organocatalysts for Asymmetric Michael Additional Reactions

References


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


PubMed Literature


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