93745-55-2

Basic information

• Product Name: 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine
• Synonyms: 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine
• CAS NO: 93745-55-2
• Molecular Formula: C₁₂H₇N₅O₃
• Molecular Weight: 269.22
• Mol File: 93745-55-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine(93745-55-2)
• EPA Substance Registry System: 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine(93745-55-2)

Safety Data

• Hazardous Substances Data: 93745-55-2(Hazardous Substances Data)

Usage

General Description

2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is a chemical compound with 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 used in organic synthesis and pharmaceutical research as a potential building block for the development of new drugs. It has been studied for its potential pharmacological activities, including its potential as an anticancer and antimicrobial agent. Additionally, it has been investigated for its potential use in the treatment of various diseases and conditions. Overall, 2-(4-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyrimidine is a versatile compound with potential applications in medicinal chemistry and drug discovery.

Upstream product

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Relevant articles and documents

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

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.

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

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.