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Di-m-tolyl-mercury, also known as bis(3-methylphenyl)mercury, is an organometallic compound with the chemical formula (C7H8)2Hg. It is a colorless, crystalline solid that is sensitive to air and moisture. di-m-tolyl-mercury is formed by the reaction of mercury with two m-tolyl (3-methylphenyl) groups, resulting in a mercury atom bonded to two aromatic rings. Di-m-tolyl-mercury is of interest in organometallic chemistry and has potential applications in various chemical synthesis processes. However, due to its toxicity and potential environmental impact, it requires careful handling and is typically used in controlled laboratory settings.

626-12-0

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626-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 626-12-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 626-12:
(5*6)+(4*2)+(3*6)+(2*1)+(1*2)=60
60 % 10 = 0
So 626-12-0 is a valid CAS Registry Number.

626-12-0Relevant academic research and scientific papers

Synthesis and Interconversion of, and Restricted Rotation in, Phenyl Complexes of Ruthenium(II)

Probitts, E. Jane,Saunders, David R.,Stone, Michael H.,Mawby, Roger J.

, p. 1167 - 1174 (2007/10/02)

The preparation and characterization of a range of phenyl complexes of ruthenium(II) are reported.For many of the complexes there is a substantial barrier to rotation of the phenyl ligand about the metal-phenyl bond, and n.m.r. studies have shown how the rate of rotation is affected by changes in the ligands in the complexes.Reaction of complexes with phosphorus or arsenic ligands L provides a convenient route to : 31P and 13C n.m.r. studies have demonstrated the sequence of steps involved and the stereochemistry of the intermediates, showing the influence of the trans-labilizing and trans-directing effects of the phenyl ligand.

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