90521-89-4 Usage
Uses
Used in Medicinal Chemistry:
(4-nitro-1H-imidazol-5-yl)(piperidin-1-yl)methanone serves as a key intermediate in the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure, which includes a reactive nitro group and a flexible piperidine ring, makes it a valuable component in the development of new drugs and therapeutic agents.
Used in Synthesis of Antimicrobial Agents:
In the field of antimicrobial chemistry, (4-nitro-1H-imidazol-5-yl)(piperidin-1-yl)methanone is used as a building block for creating new antimicrobial compounds. The nitro group's reactivity can be harnessed to form new bonds and structures that possess antimicrobial properties, contributing to the development of effective treatments against infectious diseases.
Used in the Development of Anticancer Drugs:
(4-nitro-1H-imidazol-5-yl)(piperidin-1-yl)methanone is also utilized in the development of anticancer drugs. Its structural components can be manipulated to target specific cancer cells, potentially leading to the creation of novel therapeutic agents that can combat various types of cancer.
Used in the Synthesis of CNS Active Compounds:
In the realm of central nervous system (CNS) active compounds, (4-nitro-1H-imidazol-5-yl)(piperidin-1-yl)methanone is employed as a precursor in the synthesis of molecules that can modulate CNS functions. Its structural features allow for the design of compounds that can interact with specific receptors or pathways in the CNS, potentially leading to the development of new treatments for neurological and psychiatric disorders.
Used in the Design of Radiosensitizing Agents:
(4-nitro-1H-imidazol-5-yl)(piperidin-1-yl)methanone is used in the design of radiosensitizing agents for cancer treatment. Its chemical properties can be exploited to enhance the effectiveness of radiation therapy, making it a valuable component in the development of compounds that can improve patient outcomes in cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 90521-89-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,2 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90521-89:
(7*9)+(6*0)+(5*5)+(4*2)+(3*1)+(2*8)+(1*9)=124
124 % 10 = 4
So 90521-89-4 is a valid CAS Registry Number.
90521-89-4Relevant academic research and scientific papers
Synthesis and antimicrobial activity of N,N-dialkyl-2-substituted-5-diazoimidazole-4-carboxamides
Varoli,Burnelli,Garuti,Guarnieri,Rossi
, p. 578 - 581 (2007/10/03)
A series of 2-substituted-5-diazoimidazole-4-carboxamides has been synthesized, and their antimicrobial activity has been tested in vitro. Some of the compounds show antifungal activity related to the presence of small groups on the 4-carboxamido moiety, while the presence of substituents in position 2 was detrimental.
Antitumor Imidazotetrazines. 14. Synthesis and Antitumor Activity of 6- and 8-Ssubstituted Imidazo-1,2,3,5-tetrazinones and 8-Substituted Pyrazolo-1,2,3,5-tetrazinones
Lunt, Edward,Newton, Christopher G.,Smith, Christopher,Stevens, Graham P.,Stevens, Malcolm F. G.,et al.
, p. 357 - 366 (2007/10/02)
The systematic variation of the potent antitumor agent mitozolomide (1) is extended to cover alteration of substituents at position 6 and 8 and to change the imidazo-1,2,3,5-tetrazinone (6) skeleton to the isomeric pyrazolo-1,2,3,5-tetrazino
