530081-35-7 Usage
Uses
Used in Organic Synthesis:
5-(4-Bromo-2-fluorophenyl)-2H-tetrazole is utilized as a synthetic intermediate for the creation of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, facilitating the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 5-(4-Bromo-2-fluorophenyl)-2H-tetrazole is employed as a key component in the development of new drugs. Its potential as an antitumor and antiviral agent is currently under investigation, with research focusing on its ability to target and combat cancer cells and viral infections.
Used in Antitumor Applications:
5-(4-Bromo-2-fluorophenyl)-2H-tetrazole is used as an antitumor agent for its potential to inhibit the growth and proliferation of tumor cells. 5-(4-Bromo-2-fluorophenyl)-2H-tetrazole's specific interactions with biological targets make it a promising candidate for cancer treatment.
Used in Antiviral Applications:
5-(4-Bromo-2-fluorophenyl)-2H-tetrazole also serves as an antiviral agent, where it may be used to prevent or treat viral infections by interfering with viral replication or assembly processes.
Used in Materials Science:
5-(4-Bromo-2-fluorophenyl)-2H-tetrazole may find applications in the field of materials science, where it could contribute to the development of new materials with unique properties. Its structural characteristics could be leveraged to create materials with enhanced performance in various applications.
Used as a Building Block in Functional Materials Development:
Furthermore, 5-(4-Bromo-2-fluorophenyl)-2H-tetrazole is used as a building block in the synthesis of new functional materials. Its incorporation into these materials can lead to the creation of innovative products with specialized uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 530081-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,0,0,8 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 530081-35:
(8*5)+(7*3)+(6*0)+(5*0)+(4*8)+(3*1)+(2*3)+(1*5)=107
107 % 10 = 7
So 530081-35-7 is a valid CAS Registry Number.
530081-35-7Relevant academic research and scientific papers
NOVEL COMPOUNDS AS MODULATORS OF GPR-119
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Page/Page column 75, (2013/02/27)
The present invention relates to novel compounds of formula (A) and (B) as modulators of GPR-119, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of GPR-119 mediated diseases
INDOLE SULFONAMIDE MODULATORS OF PROGESTERONE RECEPTORS
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Page/Page column 24-25, (2008/06/13)
Compounds of Formula (I), wherein n is 1 or 2, and R1, R2, R3, R4, R5, R6, R7, and R8 are as defined herein, their preparation, pharmaceutical compositions, and methods of use are disclosed.
1H-PYRROLO[2,3-B]PYRIDINES
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Page/Page column 53, (2008/06/13)
Derivatives of pyrrolo[2,3-b]pyridine which are useful as SGK-1 kinase inhibitors are described herein. The invention described herein also describes pharmaceutical compositions containing derivatives of pyrrolo[2,3-b]pyridine and methods of using pyrrolo[2,3-b]pyridine derivatives and pharmaceutical compositions thereof in the treatment of diseases mediated by SGK-1.
OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS
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Page/Page column 81-82, (2010/10/20)
The present invention relates to certain substituted phenyl oxazolidinones and to processes for the synthesis of the same. This invention also relates to pharmaceutical compositions containing the compounds of the present invention as antimicrobials. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria, for example, multiple-resistant staphylococci, streptococci and enterococci as well as anaerobic organisms, for example, Bacterioides spp. and Clostridia spp. species, and acid fast organisms, for example, Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp.