58580-09-9 Usage
Uses
Used in Biochemical and Pharmaceutical Research:
2,3-diamino-5-bromobenzoic acid dihydrochloride is utilized as a fluorescent probe or labeling agent, allowing researchers to track and visualize specific molecules or cellular components within biological systems. Its fluorescent properties make it a valuable tool in the study of molecular interactions and cellular processes.
Used in Cancer Research:
2,3-diaMino-5-broMobenzoic acid dihydrochloride is being investigated for its potential anti-cancer properties, with studies focusing on its ability to inhibit the growth of certain cancer cells. The exact mechanisms of action are still under investigation, but its potential as a therapeutic agent is promising.
Used in Anti-inflammatory Applications:
2,3-diamino-5-bromobenzoic acid dihydrochloride has shown potential as an anti-inflammatory agent, making it a candidate for further research in the treatment of inflammatory diseases. Its ability to modulate inflammatory responses could lead to new therapeutic strategies for conditions such as arthritis, asthma, and other inflammatory disorders.
Used in Drug Development:
As a compound with potential therapeutic applications, 2,3-diamino-5-bromobenzoic acid dihydrochloride is also being explored for its use in the development of new drugs. Its multifaceted properties, including its fluorescent characteristics and potential anti-cancer and anti-inflammatory effects, make it a versatile candidate for various pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 58580-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,5,8 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 58580-09:
(7*5)+(6*8)+(5*5)+(4*8)+(3*0)+(2*0)+(1*9)=149
149 % 10 = 9
So 58580-09-9 is a valid CAS Registry Number.
58580-09-9Relevant academic research and scientific papers
Process for preparing 5-halo-2,3-phenylenediamine-1-carboxylic acid
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, (2008/06/13)
Method of preparing 5-halo-2,3-phenylenediamine-1-carboxylic acids having the following formula: SPC1 Wherein X is Cl, Br or F by reacting a 2,5-dihalo-3-nitrobenzoic acid with ammonium hydroxide to yield 5-halo-3-nitro anthranilic acid followed by a redu
