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2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is a chemical compound characterized by the molecular formula C11H7N7O3. It is a yellowish solid with a molecular weight of 273.22 g/mol. 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is recognized for its potential applications in the fields of organic synthesis and pharmaceutical research, where it serves as a promising building block for the development of innovative drugs. Its pharmacological activities have been a subject of interest, with studies indicating its potential as an anticancer and antimicrobial agent. Furthermore, it has been explored for its possible utility in the treatment of a range of diseases and conditions, making it a versatile compound in the realm of medicinal chemistry and drug discovery.

93745-55-2

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93745-55-2 Usage

Uses

Used in Organic Synthesis:
2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is utilized as a key intermediate in the synthesis of complex organic molecules. Its unique structure allows for the creation of a variety of chemical entities, making it a valuable component in the development of novel compounds with potential applications in various industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is employed as a potential precursor for the design and synthesis of new drugs. Its chemical properties and reactivity contribute to the creation of drug candidates with potential therapeutic benefits.
Used in Anticancer Applications:
2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is studied for its potential as an anticancer agent, with research focusing on its ability to target and inhibit the growth of cancer cells. Its pharmacological properties make it a candidate for further investigation in the development of cancer treatments.
Used in Antimicrobial Applications:
2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is also considered for its potential antimicrobial properties, with studies exploring its effectiveness against various microorganisms. The use of 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine in antimicrobial applications could contribute to the development of new antibiotics and antifungal agents.
Used in Disease Treatment Research:
2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is investigated for its potential role in the treatment of various diseases and conditions. Its pharmacological activities are of interest to researchers seeking new therapeutic approaches for a range of health issues.

Check Digit Verification of cas no

The CAS Registry Mumber 93745-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,4 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93745-55:
(7*9)+(6*3)+(5*7)+(4*4)+(3*5)+(2*5)+(1*5)=162
162 % 10 = 2
So 93745-55-2 is a valid CAS Registry Number.

93745-55-2Downstream Products

93745-55-2Relevant academic research and scientific papers

Synthesis and antibacterial activity of some imidazo[1,2-a[pyrimidine derivatives

Rival,Grassy,Michel

, p. 1170 - 1176 (2007/10/02)

A series of 75 imidazo[1,2-a]pyrimidine derivatives were synthesized. The 'in vitro' antibacterial activity of these compounds and their corresponding α-bromoketones against a variety of gram (+), gram (-) bacteria and Mycobacterium species is reported. Some of the prepared derivatives exhibited potent antimicrobial activity.

Antifungal activity in vitro of some imidazopyrimidine derivatives

Rival, Y,Grassy, G,Taudou, A,Ecalle, R

, p. 13 - 18 (2007/10/02)

In regard to fungicidal activity of imidazole ring found in chemical compounds such as econazole, a series of 42 diversely substituted imidazopyrimidines was synthetized and examined for its antifungal activity in several species.

Convenient Synthesis of Fused Heterocycles from α-Ketohydroximoyl Chlorides and Heterocyclic Amines

Parkanyi, Cyril,Abdelhamid, Abdou O.,Cheng, John C. S.

, p. 1029 - 1032 (2007/10/02)

Nitroso derivatives of imidazopyridine (11,13,14), imidazopyrimidine (15), imidazopyrazine (16), imidazopyrazole (17), and imidazo-1,2,4-triazole (19) were obtained in good yields from α-ketohydroximoyl chlorides 3 and 2-aminopyrazines (4-6), 2-aminopyrimidine (7), 2-aminopyrazine (8), 5-amino-3-phenylpyrazole (9), and 3-amino-2H-1,2,4-triazole (10), respectively.Under different conditions, the reaction of 3 with 3-amino-2H-1,2,4-triazole (10) and 2-aminopyrazine (8) afforded the noncyclized substitution products 18 and 22, respectively.The structures of the products were assigned and confirmed on the basis of their elemental analyses, spectral data, and alternate synthesis wherever possible.

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