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CAS RN: 390766-89-9 | Product Number: B4137
(2R,5R)-(+)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone
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Purity: >97.0%(GC)
Synonyms:
- (2R,5R)-(+)-5-Benzyl-2-tert-butyl-3-methyl-4-imidazolidinone
Product Documents:
| Size | Unit Price | Belgium | Japan* |
|---|---|---|---|
| 200MG |
64,00 €
|
1 | 35 |
| 1G |
205,00 €
|
1 | 21 |
*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).
| Product Number | B4137 |
| Purity / Analysis Method | >97.0%(GC) |
| Molecular Formula / Molecular Weight | C__1__5H__2__2N__2O = 246.35 |
| Physical State (20 deg.C) | Solid |
| Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
| CAS RN | 390766-89-9 |
| PubChem Substance ID | 468590508 |
| MDL Number | MFCD08276842 |
Specifications
| Appearance | White to Light yellow powder to crystal |
| Purity(HPLC) | min. 98.0 area% |
| Optical purity(LC) | min. 98.0 ee% |
| Melting point | 98.0 to 102.0 °C |
Properties (reference)
| Melting Point | 100 °C |
| Specific Rotation | 61° (C=1,MeOH) |
GHS
Related Laws:
Transport Information:
| HS Number | 2933299090 |
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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