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N4-Benzoylcytosine
[CAS# 26661-13-2]

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Complete supplier list of N4-Benzoylcytosine
Identification
Classification Biochemical >> Nucleoside drugs >> Nucleotides and their analogues
Name N4-Benzoylcytosine
Synonyms N-(2-Oxo-1,2-dihydro-4-pyrimidinyl)benzamide; N-(2-Oxo-3H-pyrimidin-4-yl)benzamide
Molecular Structure CAS # 26661-13-2, N4-Benzoylcytosine, N-(2-Oxo-1,2-dihydro-4-pyrimidinyl)benzamide, N-(2-Oxo-3H-pyrimidin-4-yl)benzamide
Molecular Formula C11H9N3O2
Molecular Weight 215.21
CAS Registry Number 26661-13-2
EC Number 628-907-2
SMILES C1=CC=C(C=C1)C(=O)NC2=CC=NC(=O)N2
Properties
Density 1.3±0.1 g/cm3, Calc.*
Melting point >300 ºC (dec.)
Index of Refraction 1.652, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H302-H315-H319-H332-H335    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
Acute toxicityAcute Tox.4H302
Acute toxicityAcute Tox.4H332
Acute toxicityAcute Tox.4H312
SDS Available
up Discovory and Applicatios
N4-Benzoylcytosine is a synthetic derivative of cytosine, a key nucleobase that plays a vital role in the structure of nucleic acids such as DNA and RNA. The discovery of N4-benzoylcytosine can be traced back to the mid-20th century when researchers began to explore modifications of nucleobases to enhance their properties for various applications, particularly in the field of molecular biology and medicinal chemistry. The introduction of a benzoyl group at the N4 position of cytosine alters its chemical properties, making it a valuable compound for study.

The synthesis of N4-benzoylcytosine typically involves the acylation of cytosine using benzoyl chloride or benzoyl anhydride in the presence of a suitable base. This modification provides a handle for further chemical transformations and allows researchers to explore its potential biological activities. The resulting compound retains the essential properties of cytosine while offering new avenues for research and application.

N4-benzoylcytosine has garnered attention for its potential role in nucleic acid chemistry and biochemistry. Its structure makes it a useful building block for the synthesis of nucleoside analogs, which can be employed in the development of antiviral and anticancer agents. By incorporating N4-benzoylcytosine into oligonucleotides, researchers can study its interaction with complementary DNA or RNA sequences, providing insights into the mechanisms of nucleic acid recognition and hybridization.

In addition to its applications in nucleic acid research, N4-benzoylcytosine has been investigated for its potential as a pharmaceutical agent. Its structural modifications may enhance the stability and selectivity of nucleoside analogs, contributing to the development of targeted therapies. Researchers are particularly interested in exploring the compound's efficacy against viral infections and various types of cancer, where the manipulation of nucleic acid metabolism can lead to therapeutic benefits.

Furthermore, N4-benzoylcytosine serves as a valuable tool in chemical biology for studying enzyme-substrate interactions. It can act as a substrate for specific enzymes, allowing scientists to investigate the mechanisms of enzyme catalysis and the influence of structural modifications on enzymatic activity. Such studies contribute to a deeper understanding of fundamental biochemical processes and the development of enzyme inhibitors.

The exploration of N4-benzoylcytosine is ongoing, with researchers continuously investigating its chemical properties and biological activities. Advances in synthetic methodologies and analytical techniques facilitate the discovery of novel derivatives and their applications in various fields, including drug discovery and molecular diagnostics.

In summary, N4-benzoylcytosine is a significant synthetic derivative of cytosine with a variety of applications in nucleic acid chemistry, medicinal chemistry, and chemical biology. Its discovery and ongoing study highlight the importance of nucleobase modifications in developing new therapeutic agents and understanding fundamental biological processes.
Market Analysis Reports
List of Reports Available for N4-Benzoylcytosine
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