73680-76-9 Usage
Uses
Used in Organic Synthesis:
(2-bromophenyl)-N,N,N-trimethylmethanaminium bromide is used as a phase-transfer catalyst for increasing the reaction rate and yield in various chemical processes. Its ability to transfer reactants between phases makes it a valuable tool in organic synthesis.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, (2-bromophenyl)-N,N,N-trimethylmethanaminium bromide is used as a reagent in the synthesis of various pharmaceuticals. Its catalytic properties aid in the production of a range of medicinal compounds.
Used in Agrochemical Synthesis:
Similarly, in agrochemical synthesis, (2-bromophenyl)-N,N,N-trimethylmethanaminium bromide serves as a reagent, contributing to the development of various agrochemicals that are essential for agricultural applications.
Used as an Antimicrobial and Anti-Fungal Agent:
(2-bromophenyl)-N,N,N-trimethylmethanaminium bromide has been studied for its antimicrobial and antifungal properties, making it a potential additive in industrial and medical applications where control of microbial growth is necessary.
Overall, (2-bromophenyl)-N,N,N-trimethylmethanaminium bromide is a multifaceted compound with broad applications in organic chemistry, pharmaceuticals, agrochemicals, and as an antimicrobial agent.
Check Digit Verification of cas no
The CAS Registry Mumber 73680-76-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,8 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 73680-76:
(7*7)+(6*3)+(5*6)+(4*8)+(3*0)+(2*7)+(1*6)=149
149 % 10 = 9
So 73680-76-9 is a valid CAS Registry Number.
73680-76-9Relevant academic research and scientific papers
Ion Pair-Directed Regiocontrol in Transition-Metal Catalysis: A Meta-Selective C-H Borylation of Aromatic Quaternary Ammonium Salts
Davis, Holly J.,Mihai, Madalina T.,Phipps, Robert J.
supporting information, p. 12759 - 12762 (2016/10/13)
The use of noncovalent interactions to direct transition-metal catalysis is a potentially powerful yet relatively underexplored strategy, with most investigations thus far focusing on using hydrogen bonds as the controlling element. We have developed an ion pair-directed approach to controlling regioselectivity in the iridium-catalyzed borylation of two classes of aromatic quaternary ammonium salts, leading to versatile meta-borylated products. By examining a range of substituted substrates, this provides complex, functionalized aromatic scaffolds amenable to rapid diversification and more broadly demonstrates the viability of ion-pairing for control of regiochemistry in transition-metal catalysis.
Alkylation of rhodium porphyrins using ammonium and quinolinium salts
Thompson, Samuel J.,Dong, Guangbin
supporting information, p. 3757 - 3767 (2014/08/18)
Alkylation of rhodium(III) porphyrins [RhIII(por)] was achieved under relatively mild conditions in up to 98% yields, where readily available ammonium and quinolinium salts were utilized as the alkylating agents. This transformation tolerates air and water, thus serving as a convenient method to prepare a variety of alkyl- and benzyl-RhIII(por) complexes. Preliminary mechanistic studies support an SN2-like reaction pathway involving a RhI(por) anion intermediate.
