Maximum quantity allowed is 999
CAS RN: 390766-89-9 | Product Number: B4137
(2R,5R)-(+)-2-tert-Butyl-3-methyl-5-benzyl-4-imidazolidinone
Purity: >97.0%(GC)
- (2R,5R)-(+)-5-Benzyl-2-tert-butyl-3-methyl-4-imidazolidinone
| Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time |
Shipping Information
|
|---|---|---|---|---|---|
| 200MG |
$75.00
|
25 | 6 | Contact Us | |
| 1G |
$262.00
|
18 | 0 | Contact Us |
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* The storage conditions are subject to change without notice.
| 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) |
Packaging and Container
|
1G-Glass Bottle with Plastic Insert (View image), 200MG-Glass Bottle with Plastic Insert (View image) |
| CAS RN | 390766-89-9 |
| PubChem Substance ID | 468590508 |
| MDL Number | MFCD08276842 |
| 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 |
| NMR | confirm to structure |
| Melting Point | 100 °C |
| Specific Rotation | 61° (C=1,MeOH) |
| H.S.code* | 2933.29-000 |

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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