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1-Trimethylsilanyloxy-4-(1-trimethylsilanyloxy-vinyl)-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60068-18-0

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60068-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60068-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,6 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60068-18:
(7*6)+(6*0)+(5*0)+(4*6)+(3*8)+(2*1)+(1*8)=100
100 % 10 = 0
So 60068-18-0 is a valid CAS Registry Number.

60068-18-0Relevant academic research and scientific papers

Versatile and base-free copper-catalyzed α-arylations of aromatic ketones using diaryliodonium salts

Bouquin, Maxime,Jaroschik, Florian,Taillefer, Marc

supporting information, (2021/06/11)

A ligand and base-free copper catalyzed synthetic method for the efficient α-arylation of aromatic ketones is described. In order to avoid strong bases, ketone-derived silyl enol ethers were employed. Their reaction with diaryliodonium salts as aryl source provided the intermolecular C–C coupling displaying good functional group tolerance and requiring low catalyst loading.

Thermal addition reaction of aroylketene with 1-aryl-1- trimethylsilyloxyethylenes: Aromatic substituent effects of aroylketene and aryltrimethylsilyloxyethylene on their reactivity

Saitoh,Oyama,Sakurai,Niimura,Hinata,Horiguchi,Toda,Sano

, p. 956 - 966 (2007/10/03)

The thermal addition reaction of various aroylketenes (C) generated by the thermolysis of 5-aryldioxofurans (A) to 1-aryl-1-trimethylsilyloxyethylenes gave 1,5-diarylpentane-1,3,5-triones (D) and 2,6-diaryl-4H-pyran-4-ones (E). The introduction of electron withdrawing substituents in the aroylketene and of electron donating substituents facilitated the addition reaction. The observed substituent effects and the reaction mechanism are interpreted in terms of molecular orbital analyses.

PHENOLIC COMPOUNDS FROM ROOTS OF URTICA DIOICA

Kraus, Rupert,Spiteller, Gerhard

, p. 1653 - 1659 (2007/10/02)

Root extracts from Urtica dioica were separated into several classes of compounds by extraction with organic solvents at different pH values.The phenolic fraction was analysed by GC-MS after trimethylsilylation.This procedure allowed the identification of 18 phenolic compounds as well as the detection of eight lignans.The occurrence of some of these substances in this plant was previously unknown.

Unusual Fragmentation of Trimethylsilylated Enols Derived from m- and p-Hydroxyacetophenones

Kraus, Rupert,Spiteller, Gerhard

, p. 861 - 865 (2007/10/02)

When 4-hydroxyacetophenone is treated with MSTFA the corresponding bis-trimethylsilylated enol ether (1a) is obtained.The mass spectrum of 1a is characterized by a M-1(1+) base peak.Extensive deuteration experiments revealed that the hydrogen is mainly

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