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CAS RN: 346440-54-8 | Product Number: B4138
(2S,5S)-(-)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone
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Purity: >97.0%(GC)
Synonyms:
- (2S,5S)-(-)-5-Benzyl-2-tert-butyl-3-methyl-4-imidazolidinone
Product Documents:
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 200MG |
$93.00
|
1 | 0 | Contact Us | |
| 1G |
$360.00
|
23 | 1 | Contact Us |
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to order our products. The above prices do not include freight cost, customs, and other charges to the destination.
* The storage conditions are subject to change without notice.
| Product Number | B4138 |
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) |
| Packaging and Container
|
1G-Glass Bottle with Plastic Insert (View image), 200MG-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 346440-54-8 |
| Reaxys Registry Number | 6480916 |
| PubChem Substance ID | 354334237 |
| MDL Number | MFCD03426982 |
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:
| H.S.code* | 2933.29-000 |
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
PubMed Literature
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