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bis(4-methoxyphenyl)methyl trimethylsilyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

174968-73-1

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174968-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174968-73-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,9,6 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 174968-73:
(8*1)+(7*7)+(6*4)+(5*9)+(4*6)+(3*8)+(2*7)+(1*3)=191
191 % 10 = 1
So 174968-73-1 is a valid CAS Registry Number.

174968-73-1Relevant articles and documents

Salt-Free Reduction of Nonprecious Transition-Metal Compounds: Generation of Amorphous Ni Nanoparticles for Catalytic C-C Bond Formation

Yurino, Taiga,Ueda, Yohei,Shimizu, Yoshiki,Tanaka, Shinji,Nishiyama, Haruka,Tsurugi, Hayato,Sato, Kazuhiko,Mashima, Kazushi

, p. 14437 - 14441 (2016/01/25)

A salt-free procedure for the generation of a wide variety of metal(0) particles, including Fe, Co, Ni, and Cu, was achieved using 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (1), which reduced the corresponding metal precursors under mild conditions. Notably, Ni particles formed in situ from the treatment of Ni(acac)2 (acac=acetylacetonate) with 1 in toluene exhibited significant catalytic activity for reductive C-C bond-forming reactions of aryl halides in the presence of excess amounts of 1. By examination of high-magnification transmission electron microscopy images and electron diffraction patterns, we concluded that amorphous Ni nanoparticles (Ni aNPs) were essential for the high catalytic activity.

Mg-promoted C-trifluoroacetylation of benzophenone

Maekawa, Hirofumi,Ozaki, Taro,Nishiguchi, Ikuzo

supporting information; experimental part, p. 796 - 799 (2010/03/24)

Mg-promoted reduction of benzophenones in the presence of ethyl trifluoroacetate and trimethylchlorosilane in N-methyl-2-pyrrolidinone afforded the corresponding cross-coupling products, which were easily transformed into C-trifluoroacetylated compounds o

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