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(4-nitro-1H-imidazol-1-yl)acetic acid is a chemical compound characterized by its molecular formula C5H5N3O4. It features a nitro group and an imidazole ring, which contribute to its diverse chemical properties and reactivity. (4-nitro-1H-imidazol-1-yl)acetic acid is recognized for its role as a starting material in the synthesis of pharmaceuticals and agrochemicals, as well as a building block in the preparation of various heterocyclic compounds. Its versatility as an intermediate in organic synthesis, coupled with its potential applications in medicinal chemistry and drug development, positions (4-nitro-1H-imidazol-1-yl)acetic acid as a significant compound in the field of chemistry. Furthermore, its antimicrobial and anticancer properties have garnered interest for further research and development.

59566-52-8

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59566-52-8 Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
(4-nitro-1H-imidazol-1-yl)acetic acid is used as a starting material for the synthesis of various pharmaceuticals and agrochemicals, leveraging its chemical reactivity and structural features to create a wide range of active compounds.
Used in Heterocyclic Compound Preparation:
In the field of organic chemistry, (4-nitro-1H-imidazol-1-yl)acetic acid serves as a building block for the preparation of heterocyclic compounds, which are essential in the development of new chemical entities with potential applications in various industries.
Used in Medicinal Chemistry and Drug Development:
As a versatile intermediate, (4-nitro-1H-imidazol-1-yl)acetic acid is utilized in medicinal chemistry for the development of new drugs, taking advantage of its unique structural elements to design and synthesize novel therapeutic agents.
Used in Antimicrobial Research:
(4-nitro-1H-imidazol-1-yl)acetic acid is studied for its antimicrobial properties, making it a valuable compound for the development of new antimicrobial agents to combat resistant strains of bacteria.
Used in Anticancer Research:
(4-nitro-1H-imidazol-1-yl)acetic acid is also of interest in anticancer research due to its potential to inhibit the growth of cancer cells, offering a basis for the development of new anticancer drugs.
Used in Organic Synthesis:
(4-nitro-1H-imidazol-1-yl)acetic acid is a key intermediate in organic synthesis, where it is employed to construct complex organic molecules for various applications, including but not limited to the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 59566-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,6 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59566-52:
(7*5)+(6*9)+(5*5)+(4*6)+(3*6)+(2*5)+(1*2)=168
168 % 10 = 8
So 59566-52-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N3O4/c9-5(10)2-7-1-4(6-3-7)8(11)12/h1,3H,2H2,(H,9,10)

59566-52-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-nitroimidazol-1-yl)acetic acid

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:59566-52-8 SDS

59566-52-8Relevant academic research and scientific papers

Synthesis of nitroimidazole derived oxazolidinones as antibacterial agents

Varshney, Vandana,Mishra, Nripendra N.,Shukla, Praveen K.,Sahu, Devi P.

scheme or table, p. 661 - 666 (2010/04/04)

A series of N-alkylated derivatives of nitroimidazolyl oxazolidinones 6a-i with various substituent at N-1 position of the nitroimidazole were synthesized and their in-vitro antibacterial activities were evaluated against several Gram-positive and Gram-ne

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