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Home>Supplier>Henan Grubbs Chemical Co.,Ltd>benzylidene-[1,3-bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene]-dichlororuthenium,tricyclohexylphosphane

Henan Grubbs Chemical Co.,Ltd

Henan Grubbs Chemical Co.,Ltd

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China Henan Xinxiang
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0373 3809933

Catalog No. : gl201804

benzylidene-[1,3-bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene]-dichlororuthenium,tricyclohexylphosphane

  • 246047-72-3
  • 1g
  • 98%
  • 2Day (s)
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  • Product Details & Description

Product Info

Compound benzylidene-[1,3-bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene]-dichlororuthenium,tricyclohexylphosphane
CAS No. 246047-72-3 Catalog No. gl201804 Brand
Purity 98% Packing 1g Grade
Lead Time 2Day (s) Origin Loading Port

PropertiesMore

Appearance & Physical State pink-brown to red-purple crystals or powder
Melting Point 143-149ºC

Description

Grubbs catalyst, Grubbs 2nd catalyst, Grubbs 2nd generation catalyst,benzylidene [1,3- double (three methyl phenyl) -2- imidazoline subunit] two chloro (tricyclohexylphosphine) ruthenium, catalyst for olefin metathesis,Ruthenium catalyst

Product name: Grubbs 2nd generation catalyst

CAS No:  246047-72-3

Molecular formula: C46H65Cl2N2PRu   
Molecular weight: 848.97

Molecular structure:

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IUPAC Name: benzylidene [1,3- double (three methyl phenyl) -2- imidazoline subunit] two chloro (tricyclohexylphosphine) ruthenium
Appearance: (sensitive to air and water) Brownish red minuteness crystalline particles
Melting point: 216-220C (lit.)
Storage condition: 2-8 degree C 
Purity: ruthenium complex content 98%
Purpose: Catalytic decomposition reaction of unsaturated olefins, with a wide range of substrates, Including the requirement for space or the deactivation of olefins, such as 1,1 - Substituted olefins and,  - unsaturated carbonyl compounds. The catalytic activity improves the two orders of magnitudethan than the first generation  of Grubbs catalyst , the amount of the compound decomposition polymerization in the open loop can be reduced to one in a million. The amount of the complex decomposition reaction is only 5/10000.In some ring closing metathesis reaction in the amount is only five ten thousandths of, especially suitable for the synthesis of low tension cyclic olefins and the larger steric hindrance of multiple substituted olefins.

Application of Grubbs catalyst

Ring closing metathesis reaction

Ring-opening metathesis reaction

Polymerizaiton

Cross metathesis

Safety instructions: 26-36/37/39
Related categories: noble metal catalysts; ruthenium containing catalysts; chemical intermediates; pharmaceutical intermediates.


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benzylidene-[1,3-bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene]-dichlororuthenium,tricyclohexylphosphane

Cas No

246047-72-3

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