1667-01-2 Usage
Description
2',4',6'-Trimethylacetophenone is an organic compound characterized by its clear, colorless to light yellow liquid appearance. It is a derivative of acetophenone, with three methyl groups attached to the phenyl ring at the 2', 4', and 6' positions. 2',4',6'-TRIMETHYLACETOPHENONE is known for its unique chemical properties and versatile applications across various industries.
Uses
Used in Laboratory Chemicals:
2',4',6'-Trimethylacetophenone is used as a laboratory chemical for various research and development purposes. Its unique chemical structure makes it a valuable compound for studying organic reactions and syntheses.
Used in Chemical Synthesis:
As an intermediate for chemical synthesis, 2',4',6'-trimethylacetophenone plays a crucial role in the production of various substances. Its ability to participate in a wide range of chemical reactions allows it to be a key component in the synthesis of pharmaceuticals, fragrances, and other specialty chemicals.
Used in Manufacturing:
2',4',6'-Trimethylacetophenone is also utilized in the manufacturing process of various substances. Its versatility and reactivity make it an essential ingredient in the production of a wide array of chemical products, contributing to the development of new materials and compounds with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1667-01-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,6 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1667-01:
(6*1)+(5*6)+(4*6)+(3*7)+(2*0)+(1*1)=82
82 % 10 = 2
So 1667-01-2 is a valid CAS Registry Number.
1667-01-2Relevant articles and documents
Synthesis and catalytic properties of large-pore Sn-β and Al-free Sn-β molecular sieves
Mal,Ramaswamy
, p. 425 - 426 (1997)
Sn-β and Al-free Sn-β (large pore, 12-membered ring channels) molecular sieves prepared by hydrothermal synthesis and characterised by XRD, FTIR and sorption techniques are distinguished by their acidic and oxidation properties, in the acetylation of 1,3,5-trimethylbenzene (1,3,5-TMB) with acetyl chloride and in the oxidation of m-cresol and 1,3,5-TMB with aqueous H2O2, respectively.
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Kharasch,Morrison,Urry
, p. 368,370 (1944)
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Development of Trifluoromethanesulfonic Acid-Immobilized Nitrogen-Doped Carbon-Incarcerated Niobia Nanoparticle Catalysts for Friedel-Crafts Acylation
Yang, Xi,Yasukawa, Tomohiro,Yamashita, Yasuhiro,Kobayashi, Shū
, p. 15800 - 15806 (2021/10/25)
Heterogeneous trifluoromethanesulfonic acid-immobilized nitrogen-doped carbon-incarcerated niobia nanoparticle catalysts (NCI-Nb-TfOH) that show excellent catalytic performance with low niobium loading (1 mol %) in Friedel-Crafts acylation have been developed. These catalysts exhibit higher activity and higher tolerance to catalytic poisons compared with the previously reported TfOH-treated NCI-Ti catalysts, leading to a broader substrate scope. The catalysts were characterized via spectroscopic and microscopic studies.
Imidazolium Triflate Ionic Liquid Improves the Activity of ZnCl2 in the Synthesis of Pyrroles and Ketones
Nguyen, Hai Truong,Ngo, Dung Kim Thi,Chau, Khiem Duy Nguyen,Tran, Phuong Hoang
, p. 157 - 165 (2021/03/16)
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