Interesting facts
              Interesting Facts About 3-Methyl-5-Nitro-Imidazol-4-Amine
3-Methyl-5-nitro-imidazol-4-amine is a fascinating compound with significant implications in various fields, especially in medicinal chemistry. Below are some notable facts:
- Pharmaceutical Potential: This compound serves as a precursor in the synthesis of various pharmaceuticals, notably as an intermediate in the development of anti-parasitic and anti-fungal agents.
 - Imidazole Ring: The imidazole group is a five-membered heterocyclic ring that plays a crucial role in the biological activity of many biomolecules. It’s found in important compounds such as histidine, a vital amino acid.
 - Nitro Group Reactivity: The nitro group in this compound gives it unique chemical properties, making it a target for reduction reactions. This can lead to the formation of amines, which are often more biologically active.
 - Research Interest: The nitro-imidazole derivatives have been the subject of numerous studies due to their effectiveness against parasites and their potential role in hypoxic cell sensitization in cancer therapy.
 - Environmental Insight: Interesting to note, compounds similar to 3-methyl-5-nitro-imidazol-4-amine can be found in some environmental studies, particularly regarding soil and water contaminants due to their synthetic production.
 
In summary, 3-methyl-5-nitro-imidazol-4-amine not only provides insights into pharmaceutical development but also underscores the importance of chemical reactivity and biological applications. The ongoing research around this compound continues to pave the way for innovative therapeutic strategies.
Synonyms
          4531-54-8
          1-METHYL-4-NITRO-1H-IMIDAZOL-5-AMINE
          5-amino-1-methyl-4-nitroimidazole
          UNII-55UIE6811G
          55UIE6811G
          NSC-400013
          DTXSID70196469
          NSC 400013
          1H-Imidazol-5-amine, 1-methyl-4-nitro-
          AZATHIOPRINE IMPURITY A [EP IMPURITY]
          IMIDAZOLE, 5-AMINO-1-METHYL-4-NITRO-
          AZATHIOPRINE IMPURITY A (EP IMPURITY)
          DTXCID30118960
          813-053-7
          3-methyl-5-nitroimidazol-4-amine
          1H-Imidazol-5-amine,1-methyl-4-nitro-(9CI)
          1H-Imidazol-5-amine, 1-methyl-4-nitro-; Imidazole, 5-amino-1-methyl-4-nitro- (7CI,8CI); 1-Methyl-4-nitro-1H-imidazol-5-amine; 5-Amino-1-methyl-4-nitroimidazole; NSC 400013
          NSC400013
          3-Methyl-5-nitro-3H-imidazol-4-ylamine
          BAS 00291726
          Oprea1_562439
          SCHEMBL2871452
          GJVMTMXQJDQJSS-UHFFFAOYSA-N
          5-amino-1-methyl-4-nitroimid-azole
          STK834386
          AKOS000601547
          FA31238
          AS-76126
          1-Methyl-4-nitro-1H-imidazol-5-amine #
          CS-0151159
          D95001
          EN300-249675
          Q27261340
          Z57124101
              
Solubility of 3-methyl-5-nitro-imidazol-4-amine
The solubility of 3-methyl-5-nitro-imidazol-4-amine in various solvents can significantly influence its applications and reactivity in chemical processes. When exploring its solubility, consider the following aspects:
As 3-methyl-5-nitro-imidazol-4-amine is characterized by its polar functional groups, it can interact favorably with polar solvents, which aids in its dissolution. This characteristic enhances its bioavailability and potential efficacy in various chemical applications.
In summary, the solubility of 3-methyl-5-nitro-imidazol-4-amine plays a critical role in its functional usage, highlighting the necessity for thorough exploration under varying solvent environments and conditions.