6279-93-2 Usage
Uses
Used in Pharmaceutical Research:
(2-bromophenyl)(2,4,6-trimethylphenyl)methanone is utilized as a key component in the development of new drugs and pharmaceuticals. Its unique structure allows it to be a valuable building block in medicinal chemistry, contributing to the creation of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, (2-bromophenyl)(2,4,6-trimethylphenyl)methanone serves as a versatile intermediate, enabling the synthesis of a wide range of organic compounds. Its reactivity and structural features make it suitable for various chemical reactions, facilitating the production of complex organic molecules.
Used in Material Science:
(2-bromophenyl)(2,4,6-trimethylphenyl)methanone has been investigated for its potential applications in material science. Its properties may contribute to the development of new materials with specific characteristics, such as improved stability or novel functionalities.
Used as a Precursor in Synthesis:
(2-bromophenyl)(2,4,6-trimethylphenyl)methanone also acts as a precursor in the synthesis of various organic compounds. Its presence in the reaction mixture can lead to the formation of desired products through a series of chemical transformations, expanding the scope of organic chemistry and its applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6279-93-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6279-93:
(6*6)+(5*2)+(4*7)+(3*9)+(2*9)+(1*3)=122
122 % 10 = 2
So 6279-93-2 is a valid CAS Registry Number.
6279-93-2Relevant academic research and scientific papers
Erbium trifluoromethanesulfonate catalyzed Friedel-Crafts acylation using aromatic carboxylic acids as acylating agents under monomode-microwave irradiation
Tran, Phuong Hoang,Hansen, Poul Erik,Nguyen, Hai Truong,Le, Thach Ngoc
, p. 612 - 618 (2015/02/19)
Erbium trifluoromethanesulfonate is found to be a good catalyst for the Friedel-Crafts acylation of arenes containing electron-donating substituents using aromatic carboxylic acids as the acylating agents under microwave irradiation. An effective, rapid and waste-free method allows the preparation of a wide range of aryl ketones in good yields and in short reaction times with minimum amounts of waste.
The Use of Chemical Probes To Differentiate between Polar and SET-Hydrogen Atom Abstraction Pathways Involved in the Reduction Reaction Promoted by an 8-Al-4 Anion
Tanner, Dennis D.,Yang, C. M.
, p. 5907 - 5914 (2007/10/02)
The mechanism for the reduction of aromatic ketones and alkyl halides with lithium tetrakis(N-dihydropyridyl)aluminate was found to proceed competitively by hydride reduction and by single electron transfer (SET)-hydrogen atom abstraction processes.A series of ketyl fragmentation probes were used to differentiate the two pathways.A SET process is the dominant pathway when the ketones involved are sterically hindered or when strong electron acceptors are used as the substrates.The observation that EPR-active intermediates can be detected, or that small amounts of radical derived products are formed, demonstrates only that a SET pathway is available but cannot be used to establish the mechanism of the major product-forming reactions.
