75732-01-3 Usage
Description
Mesitylcopper(I), min. 97%, is an organometallic compound consisting of copper(I) ions and mesityl ligands. It is a versatile starting material for the synthesis of various copper(I) complexes and has applications in organic synthesis and as a reagent in chemical reactions.
Used in Chemical Synthesis Industry:
Mesitylcopper(I), min. 97%, is used as a starting material for synthesizing a variety of copper(I) complexes, such as homo and heteroleptic copper(I) complexes, including Cu(I) alkoxides, siloxides, phosphates, amides, and phosphides. These complexes have potential applications in various fields, such as catalysis, materials science, and bioinorganic chemistry.
Used in Organic Synthesis:
Mesitylcopper(I), min. 97%, is used as a selective mesityl group transfer reagent in stoichiometric C-C and C-heteroatom bond-forming reactions. This allows for the formation of new chemical bonds and the synthesis of complex organic molecules.
Used in Materials Science:
Mesitylcopper(I), min. 97%, is used to synthesize biorelevant copper(I) complexes that serve as biomimetic model compounds. These complexes can help researchers understand the structure and function of copper-containing enzymes and develop new materials with unique properties.
Used in Nanotechnology:
Mesitylcopper(I), min. 97%, can be used to synthesize copper nanoparticles from stabilizing primary amines. These nanoparticles have potential applications in various fields, such as electronics, catalysis, and medicine, due to their unique size-dependent properties.
Used in Copper Diketonate Complexes Synthesis:
Mesitylcopper(I), min. 97%, is used as an organometal in the synthesis of copper diketonate complexes. These complexes have potential applications in various fields, such as catalysis, photovoltaics, and as precursors for the synthesis of other copper-containing materials.
Check Digit Verification of cas no
The CAS Registry Mumber 75732-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,7,3 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75732-01:
(7*7)+(6*5)+(5*7)+(4*3)+(3*2)+(2*0)+(1*1)=133
133 % 10 = 3
So 75732-01-3 is a valid CAS Registry Number.
75732-01-3Relevant articles and documents
Synthesis and Reactivity of Fluoroalkyl Copper Complexes by the Oxycupration of Tetrafluoroethylene
Ohashi, Masato,Adachi, Takuya,Ishida, Naoyoshi,Kikushima, Kotaro,Ogoshi, Sensuke
, (2017)
The copper(I)-mediated generation of -OCF2CF2- moieties by the oxycupration of tetrafluoroethylene (TFE) using either copper aryloxides or alkoxides is disclosed. The key intermediates, 2-aryloxy-1,1,2,2-tetrafluoroethyl and 2-alkoxy
Enantioselective Borylative Dearomatization of Indoles through Copper(I) Catalysis
Kubota, Koji,Hayama, Keiichi,Iwamoto, Hiroaki,Ito, Hajime
supporting information, p. 8809 - 8813 (2015/11/27)
The enantioselective borylative dearomatization of a heteroaromatic compound has been achieved using a copper(I) catalyst and a diboron reagent. This reaction involves the regio- and enantioselective addition of active borylcopper(I) species to indole-2-carboxylates, followed by the diastereoselective protonation of the resulting copper(I) enolate to give the corresponding chiral indolines, which bear consecutive stereogenic centers.
Isolation and X-ray crystal structures of triarylphosphine radical cations
Pan, Xiaobo,Chen, Xiaoyu,Li, Tao,Li, Yizhi,Wang, Xinping
supporting information, p. 3414 - 3417 (2013/04/23)
Salts containing triarylphosphine radical cations 1?+ and 2?+ have been isolated and characterized by electron paramagnetic resonance (EPR) and UV-vis absorption spectroscopy as well as single-crystal X-ray diffraction. Radical 1?+ exhibits a relaxed pyramidal geometry, while radical 2?+ becomes fully planar. EPR studies and theoretical calculations showed that the introduction of bulky aryl groups leads to enhanced p character of the singly occupied molecular orbital, and the radicals become less pyramidalized or fully flattened.