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4-(Nitrophenyl) 4-guanidinobenzoate

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Identification
Molecular formula
C14H12N4O4
CAS number
57675-96-4
IUPAC name
(4-nitrophenyl) 4-guanidinobenzoate
State
State

At room temperature, (4-nitrophenyl) 4-guanidinobenzoate exists as a solid. It is typically stored in sealed containers to avoid moisture uptake and protect it from degradation.

Melting point (Celsius)
154.00
Melting point (Kelvin)
427.15
Boiling point (Celsius)
314.00
Boiling point (Kelvin)
587.15
General information
Molecular weight
315.30g/mol
Molar mass
315.3030g/mol
Density
1.3500g/cm3
Appearence

The compound typically appears as a crystalline solid. It can range in color from white to a light yellow, depending on its purity and the presence of impurities. The structure of the compound involves aromatic rings which contribute to its stability and specific visual characteristics.

Comment on solubility

Solubility of (4-nitrophenyl) 4-guanidinobenzoate

The solubility of (4-nitrophenyl) 4-guanidinobenzoate is an intriguing topic due to the compound's complex structure and functional groups. This molecule exhibits some unique solubility characteristics:

  • Polarity: The presence of the nitro group and the guanidine moiety significantly influences its polarity, potentially enhancing solubility in polar solvents like water.
  • Hydrogen Bonding: The guanidine portion can form hydrogen bonds, which may improve solubility through interactions with solvent molecules.
  • Organic Solvents: While it may dissolve well in polar organic solvents such as methanol and ethanol, its solubility in non-polar solvents is likely to be minimal.
  • pH Dependence: The solubility can be affected by the pH of the solvent, as the guanidine group can be protonated or deprotonated, altering its solubility characteristics.

In conclusion, the solubility of (4-nitrophenyl) 4-guanidinobenzoate is a multifaceted property that is largely influenced by its functional groups, polarity, and environmental factors. As expressed by many chemists: "Understanding the solubility of compounds is key to unlocking their potential applications."

Interesting facts

Interesting Facts about (4-Nitrophenyl) 4-Guanidinobenzoate

(4-Nitrophenyl) 4-guanidinobenzoate is a fascinating compound that has garnered attention due to its unique structure and chemical properties. It falls under the category of guanidine derivatives, which are known for their diverse biological activity and are often used in pharmaceutical applications.

Key Properties and Applications

  • Biological Activity: This compound exhibits notable antibacterial and antiviral properties, making it a subject of interest in the development of new antibiotics and antiviral drugs.
  • pH Sensitivity: The guanidine group allows the compound to be pH-sensitive, which is beneficial for targeted drug delivery systems and controlled release formulations.
  • Research Interest: Its ability to act as a biochemical probe in scientific research is noteworthy, especially in studies related to enzyme inhibition and receptor interactions.

Chemical Characteristics

The presence of the nitrophenyl group contributes to the electron-withdrawing nature of the compound, affecting its reactivity and interaction with biological molecules. This unique combination of functional groups enhances its efficacy in various chemical reactions and biological applications.

A Quote to Remember

As researchers delve deeper into the realm of organic chemistry, compounds like (4-nitrophenyl) 4-guanidinobenzoate remind us that "the complexities of nature often lead to innovative solutions." — Unknown Scientist

In conclusion, (4-nitrophenyl) 4-guanidinobenzoate represents a bridge between organic chemistry and pharmaceutical science, highlighting the potential of tailored compounds in addressing modern health challenges. Its ongoing study is sure to yield exciting discoveries in the near future.

Synonyms
21658-26-4
4-Nitrophenyl 4'-guanidinobenzoate
XT3X7GT7P2
DTXSID90176041
Benzoic acid, 4-((aminoiminomethyl)amino)-, 4-nitrophenyl ester
4-Nitrophenyl 4-((aminoiminomethyl)amino)benzoate
4-Nitrophenyl 4-[(aminoiminomethyl)amino]benzoate
Benzoic acid, 4-[(aminoiminomethyl)amino]-, 4-nitrophenyl ester
RefChem:912723
DTXCID2098532
p-nitrophenyl p'-guanidinobenzoate
4-nitrophenyl p'-guanidinobenzoate
para-nitrophenyl p'-guanidinobenzoate
4-Nitrophenyl 4-guanidinobenzoate
(4-nitrophenyl) 4-(diaminomethylideneamino)benzoate
CHEMBL550687
NPGB (hydrochloride)
Nitrophenyl p-guanidinobenzoate
p-Nitrophenyl p-guanidino-benzoate
p-Nitrophenyl-p'-guanidinobenzoate
p-Nitrophenyl-p'-guanidino benzoate
BRN 2819493
p-Guanidinobenzoic acid p-nitrophenyl ester
SCHEMBL237695
BENZOIC ACID, p-GUANIDINO-, p-NITROPHENYL ESTER
p-nitrophenyl p-guanidinobenzoate
SCHEMBL29358345
BDBM33249
CFOQGBUQTOGYKI-UHFFFAOYSA-N
(4-nitrophenyl) 4-guanidinobenzoate
BDBM50069132
MFCD00152149
AKOS037651926
4-nitrophenyl 4-carbamimidamidobenzoate, 2
F95542
Z275254970