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CAS RN: 502964-52-5 | Product Number: N1060

nitro-Grela


Purity: >97.0%(HPLC)
Synonyms:
  • [1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro[(2-isopropoxy-5-nitrobenzylidene)]ruthenium(II)
Documents:
100MG
$208.00
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500MG
$625.00
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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
CAS RN 502964-52-5
Reaxys Registry Number 19324055
PubChem Substance ID 354334037
MDL Number

MFCD28411645

Specifications
Appearance Green to Dark green powder to crystal
Purity(HPLC) min. 97.0 area%
Elemental analysis(Nitrogen) 5.90 to 6.50 %
Properties (reference)
GHS
Related Laws:
Transport Information:
HS Number 2931.90.6000
Application
TCI Practical Example: Olefin Metathesis Using nitro-Grela

Used Chemicals

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


Application
Nitro-Grela: A Metathesis Catalyst Applicable to Macrocycle construction

Reference


Application
Nitro-Grela: A Metathesis Catalyst Applicable to Various Substrates

References


Application
Nitro-Grela: A Ruthenium Complex Useful for Metathesis Reactions

Experimental procedure2): A mixture of 1 (25.0 mg, 69.3 µmol) and nitro-Grela (929 µg, 1.39 µmol) in CH2Cl2 (3.5 mL) is stirred at room temperature for 2 h. The mixture is concentrated to give a residue, which is subjected to column chromatography on silica gel. Elution with hexane:ethyl acetate (10:1) gives 2 (15.6 mg, 74% yield) as a colorless oil.

References


Documents (Note: Some products will not have analytical charts available.)
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