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CAS RN: 346440-54-8 | Product Number: B4138
(2S,5S)-(-)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone
Purity: >97.0%(GC)
Synonyms:
- (2S,5S)-(-)-5-Benzyl-2-tert-butyl-3-methyl-4-imidazolidinone
Documents:
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
200MG |
€81.00
|
1 | ≥20 |
|
1G |
€315.00
|
2 | ≥20 |
|
*Stock available in Belgium will be delivered in 1 to 3 days
*Stock available in Japan will be delivered in 1 to 2 weeks (excludes regulated items and dry ice shipments).
Specifications
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Optical purity(LC) | min. 98.0 ee% |
Melting point | 97.0 to 101.0 °C |
Properties (reference)
Melting Point | 100 °C |
Specific Rotation | -60° (C=1,MeOH) |
GHS
Related Laws:
Transport Information:
HS Number | 2933790090 |
Application
Imidazolidinone Derivatives for Versatile Asymmetric Reactions
References
- 1) The First Enantioselective Organocatalytic Mukaiyama-Michael Reaction: A Direct Method for the Synthesis of Enantioenriched γ-Butenolide Architecture
- 2) Enantioselective organocatalytic epoxidation using hypervalent iodine reagents
- 3) Enantioselective Organocatalytic Singly Occupied Molecular Orbital Activation: The Enantioselective α-Enolation of Aldehydes
- 4) Enantioselective Organocatalytic Intramolecular Diels−Alder Reactions. The Asymmetric Synthesis of Solanapyrone D
- 5) Total Synthesis of (−)-Spinosyn A via Carbonylative Macrolactonization
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