7017-48-3 Usage
Uses
Used in Pharmaceutical Synthesis:
5-BROMO-2-METHOXYPHENYLACETIC ACID is used as a key intermediate in the synthesis of pharmaceutical drugs and organic compounds. Its unique structure allows for the creation of a variety of medicinal agents, contributing to the development of new treatments for different health conditions.
Used in Antifungal Applications:
5-BROMO-2-METHOXYPHENYLACETIC ACID is studied for its potential antifungal properties, making it a candidate for use in treatments targeting fungal infections. Its ability to inhibit fungal growth could be beneficial in managing and preventing various fungal-related diseases.
Used in Antibacterial Applications:
Similarly, 5-BROMO-2-METHOXYPHENYLACETIC ACID is being investigated for its potential antibacterial properties. If proven effective, 5-BROMO-2-METHOXYPHENYLACETIC ACID could be utilized in the development of new antibiotics to combat bacterial infections, particularly in the context of increasing antibiotic resistance.
Used in Medical Treatment Research:
5-BROMO-2-METHOXYPHENYLACETIC ACID is also being explored for its potential use in the treatment of various medical conditions. While the exact mechanisms and specific applications are still under investigation, its unique chemical structure suggests it may have therapeutic benefits in a range of health areas.
Check Digit Verification of cas no
The CAS Registry Mumber 7017-48-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7017-48:
(6*7)+(5*0)+(4*1)+(3*7)+(2*4)+(1*8)=83
83 % 10 = 3
So 7017-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO3/c1-13-8-3-2-7(10)4-6(8)5-9(11)12/h2-4H,5H2,1H3,(H,11,12)
7017-48-3Relevant academic research and scientific papers
Lipophilic versus hydrogen-bonding effect in P3 on potency and selectivity of valine aspartyl ketones as caspase 3 inhibitors
Mellon, Christophe,Aspiotis, Renee,Black, Cameron W.,Bayly, Christopher I.,Grimm, Erich L.,Giroux, Andre,Han, Yongxin,Isabel, Elise,McKay, Daniel J.,Nicholson, Donald W.,Rasper, Dita M.,Roy, Sophie,Tam, John,Thornberry, Nancy A.,Vaillancourt, John P.,Xanthoudakis, Steven,Zamboni, Robert
, p. 3886 - 3890 (2007/10/03)
Caspase 3 is a cysteinyl protease that mediates apoptotic cell death. Its inhibition may have an important impact in the treatment of several degenerative diseases. The P1 aspartic acid residue is a required element of recognition for this enzy
Application of the Suzuki Biphenyl Synthesis to the Natural Products Biphenomycin and Vancomycin
Brown, Allan G.,Crimmin, Michael J.,Edwards, Peter D.
, p. 123 - 130 (2007/10/02)
The synthesis of the unsymmetrical biphenyls 10 and 25 has been carried out by the palladium(0) catalysed coupling of the aryl boronic derivatives 5 and 20 with the aryl bromides 9 and 23 derived from (R)-4-hydroxyphenylglycine and (S)-tyrosine.In the former case unsuccessful attempts were made to bring about cyclization to compound 4 which is an analogue of the biphenyl ring system found in vancomycin.In the latter case, a variety of cyclization methods were used to give the cyclic products 34 and 35 which are analogues of the biphenomycin antibiotics.
