Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1346137-04-9

Post Buying Request

1346137-04-9 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1346137-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1346137-04-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,6,1,3 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1346137-04:
(9*1)+(8*3)+(7*4)+(6*6)+(5*1)+(4*3)+(3*7)+(2*0)+(1*4)=139
139 % 10 = 9
So 1346137-04-9 is a valid CAS Registry Number.

1346137-04-9Relevant articles and documents

Synthesis and catalytic evaluation of ruthenium-arene complexes bearing imidazol(in)ium-2-thiocarboxylate ligands

Hans, Morgan,Willem, Quentin,Wouters, Johan,Demonceau, Albert,Delaude, Lionel

, p. 6133 - 6142 (2012/01/04)

Five new complexes with the generic formula [RuCl2(p-cymene) (SOC·NHC)] (2-6) were isolated in high yields by reacting the [RuCl 2(p-cymene)]2 dimer with a range of imidazol(in)ium-2- thiocarboxylate zwitterions bearing cyclohexyl, 2,4,6-trimethylphenyl (mesityl), or 2,6-diisopropylphenyl groups on their nitrogen atoms in CH 2Cl2 at -20 °C. All the products were fully characterized by IR and NMR spectroscopy, and the molecular structures of [RuCl2(p-cymene)(SOC·IMes)] (3) and [RuCl2(p- cymene)(SOC·SIMes)] (5) were determined by X-ray diffraction analysis. Coordination of the NHC·COS ligands took place via the sulfur atom. A remarkable shielding of the methine proton on the p-cymene isopropyl group was observed by 1H NMR spectroscopy for complexes 3-6. It is most likely caused by the aromatic ring current of a neighboring mesityl or 2,6-diisopropylphenyl substituent. The catalytic activity of compounds 2-6 was probed in the ring-opening metathesis polymerization (ROMP) of cyclooctene, in the atom transfer radical polymerization (ATRP) of methyl methacrylate, and in the synthesis of enol esters from 1-hexyne and 4-acetoxybenzoic acid. In all these reactions, the [RuCl2(p-cymene)(SOC·NHC)] complexes displayed performances slightly inferior to those exhibited by [RuCl 2(p-cymene)(NHC)] species that result from the reaction of [RuCl 2(p-cymene)]2 with NHC·CO2 inner salts. However, they were significantly better catalyst precursors than the much more robust chelates of the [RuCl(p-cymene)(S2C·NHC)]PF6 type obtained by coordination of NHC·CS2 betaines to the ruthenium dimer. These results suggest that the Ru-(SOC·NHC) motif undergoes a dethiocarboxylation under the experimental conditions adopted for the catalytic tests and leads to the same elusive Ru-NHC active species as the preformed [RuCl2(p-cymene)(NHC)] family of complexes.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1346137-04-9