18649-43-9 Usage
Description
Used in Chemical and Industrial Applications:
(4-methoxyphenyl)-lambda~2~-plumbanyl acetic acid (1:3) is used as a component in the manufacturing of organic compounds, contributing to the synthesis of various chemical products.
Used in Catalysts for Chemical Reactions:
(4-methoxyphenyl)-lambda~2~-plumbanyl acetic acid (1:3) also serves as a catalyst in chemical reactions, facilitating and enhancing the rate of specific processes in the chemical industry.
Used in Materials Science:
(4-methoxyphenyl)-lambda~2~-plumbanyl acetic acid (1:3) is utilized in the field of materials science for its potential to create new functional materials, thanks to its distinctive coordination properties.
Used in Nanotechnology:
In nanotechnology, this compound has potential applications due to its unique coordination chemistry, which can be harnessed to develop advanced materials and devices at the nanoscale.
It is crucial to handle (4-methoxyphenyl)-lambda~2~-plumbanyl acetic acid (1:3) with care, as lead compounds can be toxic. Proper safety precautions should be taken when working with this compound to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 18649-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,6,4 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18649-43:
(7*1)+(6*8)+(5*6)+(4*4)+(3*9)+(2*4)+(1*3)=139
139 % 10 = 9
So 18649-43-9 is a valid CAS Registry Number.
18649-43-9Relevant articles and documents
Enantioselective construction of sterically hindered tertiary α-aryl ketones: A catalytic asymmetric synthesis of isoflavanones
Carroll, Michael P.,Mueller-Bunz, Helge,Guiry, Patrick J.
supporting information, p. 11142 - 11144 (2013/01/15)
A method for the catalytic asymmetric α-arylation of ketones bearing very sterically hindered aryl rings has been developed. This reaction occurs under mild conditions, in short reaction times and has been applied to the first catalytic asymmetric synthesis of isoflavanones.
Reaction of Arylboronic Acids and their Derivatives with Lead Tetra-acetate. The Generation of Aryl-lead Triacetates, and meta- and para-Phenylenebis(lead triacetate), in situ for Electrophilic Arylation
Morgan, Jacqueline,Pinhey, John T.
, p. 715 - 720 (2007/10/02)
Arylboronic acids and some of their derivatives have been found to undergo a rapid boron-lead exchange with lead tetra-acetate.In the presence of a catalytic amount of mercury(II) acetate, the reaction produces mainly the aryl-lead triacetate, and it has been developed as a convenient method for in situ generation of these useful electrophilic C-arylating reagents.The reaction allows the generation for the first time of meta- and para-phenylenebis(lead triacetate), compounds which behave as meta- and para-phenylene dication equivalents.