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Identification
Molecular formula
C14H13N5O2S
CAS number
Not Available
IUPAC name
1-(diaminomethylene)-2-[4-(4-nitrophenyl)sulfanylphenyl]guanidine
State
State

At room temperature, this compound is typically found in a solid state.

Melting point (Celsius)
250.00
Melting point (Kelvin)
523.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
357.38g/mol
Molar mass
357.3820g/mol
Density
1.5600g/cm3
Appearence

This compound appears as a crystalline solid that can vary in color from light yellow to orange due to the presence of the nitro group.

Comment on solubility

Solubility of 1-(diaminomethylene)-2-[4-(4-nitrophenyl)sulfanylphenyl]guanidine

The solubility of the compound 1-(diaminomethylene)-2-[4-(4-nitrophenyl)sulfanylphenyl]guanidine can be analyzed based on its structural characteristics. This molecule, which contains multiple functional groups, exhibits varying solubility in different solvents. Key points to consider include:

  • Polarity: The presence of amine groups and a nitro group can contribute to polar interactions, enhancing solubility in polar solvents like water.
  • Aromatic ring systems: The aromatic structures present may lead to reduced solubility in polar solvents but can improve compatibility with organic solvents such as ethanol or acetone.
  • Hydrogen bonding: The potential for hydrogen bonding due to the presence of nitrogen and sulfur moieties can significantly affect solubility, often allowing for increased solvation in polar environments.

Overall, the solubility of this compound is likely to be moderate in polar solvents but may vary significantly in non-polar environments. As with many complex organic molecules, empirical testing is necessary to determine specific solubility values.

Interesting facts

Interesting Facts about 1-(Diaminomethylene)-2-[4-(4-nitrophenyl)sulfanylphenyl]guanidine

1-(Diaminomethylene)-2-[4-(4-nitrophenyl)sulfanylphenyl]guanidine is a fascinating compound that showcases the versatility of guanidine derivatives in various applications. Here are some interesting insights into this compound:

  • Guanidine Backbone: The presence of the guanidine moiety makes this compound relevant in medicinal chemistry, particularly in the development of pharmaceuticals due to its basic nature and ability to form bonds with various receptors.
  • Functional Groups: The inclusion of nitrophenyl and sulfanyl groups introduces significant electronic and steric properties, which can influence the compound's reactivity and interactions. These refinements can result in enhanced bioactivity or unique chemical behavior.
  • Potential Applications: Compounds with a similar structure have been investigated for their roles in:
    • Agriculture as pesticides or herbicides
    • Pharmaceuticals targeting specific biological pathways
    • Dyes and pigments due to the vibrant interaction of the nitrophenyl group
  • Research Significance: Scientists are continually exploring guanidine derivatives for their potential to stabilize proteins and as ligands in coordination chemistry, showcasing a broad scope for research and development.
  • Environmental Impact: While conducting research, it is important to also consider the implications of synthesizing and utilizing such compounds in terms of environmental toxicity and sustainability.

Overall, 1-(Diaminomethylene)-2-[4-(4-nitrophenyl)sulfanylphenyl]guanidine stands out as an excellent example of how modifying molecular structures can lead to diverse functionalities and applications in science.

Synonyms
20567-00-4
BRN 2176302
BIGUANIDE, 1-(p-((p-NITROPHENYL)THIO)PHENYL)-
T-1212
1-(p-((p-Nitrophenyl)thio)phenyl)biguanide
N-(4-((4-Nitrophenyl)thio)phenyl)imidodicarbonimidic diamide
DTXSID20174570
Imidodicarbonimidic diamide, N-(4-((4-nitrophenyl)thio)phenyl)-
DTXCID2097061
RefChem:329450