Published TCIMAIL newest issue No.196
Maximum quantity allowed is 999
CAS RN: 502964-52-5 | Product Number: N1060
nitro-Grela
Purity: >97.0%(HPLC)
- [1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro[(2-isopropoxy-5-nitrobenzylidene)]ruthenium(II)
Size | Unit Price | Belgium | Japan* | Quantity |
---|---|---|---|---|
100MG |
£149.00
|
1 | 33 |
|
500MG |
£474.00
|
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).
Supplemental Product Information:
Sold in collaboration with Apeiron Synthesis.
PCT/EP2003/011222
Product Number | N1060 |
Purity / Analysis Method | >97.0%(HPLC) |
Molecular Formula / Molecular Weight | C__3__1H__3__7Cl__2N__3O__3Ru = 671.63 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Room Temperature (Recommended in a cool and dark place, <15°C) |
CAS RN | 502964-52-5 |
Reaxys Registry Number | 19324055 |
PubChem Substance ID | 354334037 |
MDL Number | MFCD28411645 |
Appearance | Green to Dark green powder to crystal |
Purity(HPLC) | min. 97.0 area% |
HS Number | 2843909000 |
Used Chemicals
- Diethyl Diallylmalonate [D1183]
- nitro-Grela [N1060]
- Dichloromethane
Procedure
In a 200 mL two necked round bottomed flask, nitro-Grela (15 mg, 22 µmol) was added, and purged with N2. Dichloromethane (40 mL) was charged in the flask, and diethyl diallylmalonate (237 mg, 986 µmol) in dichloromethane (5.5 mL) was added dropwise and the mixture was stirred at room temperature for 6 h. The solvent was removed under reduced pressure and the residue was purified by silica-gel column chromatography (hexane : EtOAc = 1 : 1) to give diethyl cyclopent-3-ene-1,1-dicarboxylate as a pale yellow oil (206 mg, 98%).
Experimenter's Comments
The reaction mixture was monitored by NMR.
Analytical Data(Diethyl cyclopent-3-ene-1,1-dicarboxylate)
1H NMR (400 MHz, CDCl3); δ 5.61 (s, 2H), 4.20 (q, J = 8.0 Hz, 4H), 3.01 (s, 4H), 1.25 (t, J = 8.0 Hz, 6H).
Lead Reference
- Nitro-Substituted Hoveyda−Grubbs Ruthenium Carbenes: Enhancement of Catalyst Activity through Electronic Activation
Reference
- Total Synthesis of Mycalolides A and B through Olefin Metathesis
References
- A Highly Efficient Ruthenium Catalyst for Metathesis Reactions
- In an Attempt to Provide a User's Guide to the Galaxy of Benzylidene, Alkoxybenzylidene, and Indenylidene Ruthenium Olefin Metathesis Catalysts
References
- 1)A Highly Efficient Ruthenium Catalyst for Metathesis Reactions
- 2)First Diastereoselective Chiral Synthesis of (-)-Securinine
Articles/Brochures
[TCI Practical Example] Olefin Metathesis Using nitro-Grela
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