Interesting facts
Interesting Facts about 1-(Diaminomethylene)-2-(2-furylmethyl)guanidine
1-(Diaminomethylene)-2-(2-furylmethyl)guanidine is a fascinating compound with unique structural features that enhance its chemical properties. Here are some intriguing aspects:
- Structure-Activity Relationship: This compound contains both guanidine and furyl functional groups. The molecular structure allows for interesting interactions with biological systems, making it a subject of study in medicinal chemistry.
- Biological Relevance: Several derivatives of guanidine compounds have been explored for their pharmacological activities, such as their antimicrobial and antiviral properties. This compound may thus exhibit similar potential.
- Versatile Reactivity: The presence of the diamino group in this molecule enhances its nucleophilicity, allowing it to participate in various organic reactions, including condensation and substitution.
- Sustainability in Research: The synthesis of furyl-containing compounds is gaining attention in green chemistry, as many derivatives are derived from renewable resources. This makes 1-(diaminomethylene)-2-(2-furylmethyl)guanidine a candidate for sustainable synthetic approaches.
- Exploratory Applications: Due to its unique structural attributes, researchers are interested in investigating its potential applications in the development of novel therapeutics, agrochemicals, and functional materials.
In summary, 1-(diaminomethylene)-2-(2-furylmethyl)guanidine is more than just a chemical compound. Its intriguing properties and potential applications signify it as a compound worthy of deeper investigation in the realms of both chemistry and pharmacology.
Synonyms
Furfuryl Biguanide
7644-42-0
DTXSID30274696
DTXCID10226158
Maybridge1_003898
N-furfurylbiguanide
SCHEMBL6695378
CHEMBL5267818
WXIHLCZQQGEOKH-UHFFFAOYSA-N
NSC756972
NSC-756972
Solubility of 1-(diaminomethylene)-2-(2-furylmethyl)guanidine
The solubility of 1-(diaminomethylene)-2-(2-furylmethyl)guanidine can be influenced by various factors including its molecular structure and the polarity of its functional groups. Generally, guanidine derivatives are known for their polar characteristics, which can enhance their solubility in polar solvents such as:
In contrast, they typically display lower solubility in non-polar solvents. The presence of both diamine and furyl moieties can also impact its solubility profile. As a result, one can expect the following:
In addition, compounds similar to 1-(diaminomethylene)-2-(2-furylmethyl)guanidine exhibit solubility characteristics that suggest ionic interactions could play a role in their dissolving behavior. This complex interplay of molecular interactions emphasizes the importance of considering both the functional groups present and the solvent environment when evaluating solubility.