64328-68-3 Usage
Uses
Used in Organic Synthesis:
2-BROMO-1-(4-PENTYLPHENYL)ETHAN-1-ONE is used as a key intermediate in organic synthesis for the production of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Research:
In the field of chemical research, 2-BROMO-1-(4-PENTYLPHENYL)ETHAN-1-ONE serves as a model compound for studying the reactivity and properties of aromatic ketones. Its specific structure and properties make it an ideal candidate for investigating reaction mechanisms, exploring new synthetic routes, and developing innovative methodologies in organic chemistry.
Used in Pharmaceutical Industry:
2-BROMO-1-(4-PENTYLPHENYL)ETHAN-1-ONE may have potential applications in the pharmaceutical industry as a precursor for the synthesis of bioactive compounds. Its unique structure can be further modified to develop new drugs with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Building Blocks for Other Organic Compounds:
Due to its specific structure and properties, 2-BROMO-1-(4-PENTYLPHENYL)ETHAN-1-ONE can be used as a building block in the production of other organic compounds. Its versatility in chemical reactions allows for the creation of a wide range of compounds with diverse applications in various industries, including materials science, agrochemicals, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 64328-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,2 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64328-68:
(7*6)+(6*4)+(5*3)+(4*2)+(3*8)+(2*6)+(1*8)=133
133 % 10 = 3
So 64328-68-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H17BrO/c1-2-3-4-5-11-6-8-12(9-7-11)13(15)10-14/h6-9H,2-5,10H2,1H3
64328-68-3Relevant academic research and scientific papers
Identification of Anti-Mycobacterial Biofilm Agents Based on the 2-Aminoimidazole Scaffold
Nguyen, T. Vu,Minrovic, Bradley M.,Melander, Roberta J.,Melander, Christian
, p. 927 - 937 (2019/03/26)
Tuberculosis (TB) remains a significant global health problem for which new therapeutic options are sorely needed. The ability of the causative agent, Mycobacterium tuberculosis, to reside within host macrophages and form biofilm-like communities contributes to the persistent and drug-tolerant nature of the disease. Compounds that can prevent or reverse the biofilm-like phenotype have the potential to serve alongside TB antibiotics to overcome this tolerance, and decrease treatment duration. Using Mycobacterium smegmatis as a surrogate organism, we report the identification of two new 2-aminoimidazole compounds that inhibit and disperse mycobacterial biofilms, work synergistically with isoniazid and rifampicin to eradicate preformed M. smegmatis biofilms in vitro, are nontoxic toward Galleria mellonella, and exhibit stability in mouse plasma.
The chemical synthesis and antibiotic activity of a diverse library of 2-aminobenzimidazole small molecules against MRSA and multidrug-resistant A. baumannii
Huigens III, Robert W.,Reyes, Samuel,Reed, Catherine S.,Bunders, Cynthia,Rogers, Steven A.,Steinhauer, Andrew T.,Melander, Christian
supporting information; experimental part, p. 663 - 674 (2010/05/02)
Multidrug-resistant bacterial infections continue to be a rising global health concern. Herein is described the development of a class of novel 2-aminobenzimidazoles with antibiotic activity. These active 2-aminobenzimidazoles retain their antibiotic activity against several strains of multidrug-resistant Staphylococcus aureus and Acinetobacter baumannii when compared to susceptible strains.
