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Phenylphenylcarbamoylaminourea

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Identification
Molecular formula
C13H12N4O
CAS number
531-85-1
IUPAC name
1-anilino-3-phenylimino-urea
State
State
Solid at room temperature.
Melting point (Celsius)
221.00
Melting point (Kelvin)
494.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.00
General information
Molecular weight
225.26g/mol
Molar mass
225.2450g/mol
Density
1.2670g/cm3
Appearence
Solid, light yellow to white crystalline powder.
Comment on solubility

Solubility of 1-anilino-3-phenylimino-urea

The solubility of 1-anilino-3-phenylimino-urea is influenced by several key factors:

  • Polarity: As a compound that contains both an aniline and an imino group, its polarity can affect its ability to dissolve in various solvents.
  • Hydrogen Bonding: The presence of hydrogen bond donors and acceptors indicates that this compound can engage in hydrogen bonding, which can enhance solubility in polar solvents, especially water.
  • Solvent Choice: This compound tends to have better solubility in organic solvents like ethanol and acetone compared to less polar solvents.

In summary, 1-anilino-3-phenylimino-urea demonstrates variable solubility predominantly governed by its polar characteristics and the nature of the solvent used. It is essential to consider these parameters when attempting to dissolve this compound effectively.

Interesting facts

Interesting Facts about 1-anilino-3-phenylimino-urea

1-anilino-3-phenylimino-urea is an intriguing compound that showcases the fascinating world of organic chemistry. Here are some compelling facts about this unique compound:

  • 1-anilino-3-phenylimino-urea belongs to a class of compounds known as ureas, which play a significant role in various biological processes. Ureas are essential in the chemistry of life, notably in protein synthesis and metabolism.
  • This compound features an aniline structure, which is derived from benzene and is one of the simplest aromatic amines. Aniline and its derivatives are widely used in the production of dyes, plastics, and pharmaceuticals.
  • The compound is characterized by the presence of both an aniline group and a phenyl group, resulting in a molecular structure that can exhibit fascinating intermolecular interactions. These interactions can influence the compound's properties and potential applications.
  • 1-anilino-3-phenylimino-urea has attracted attention in medicinal chemistry, as compounds with similar structures have shown antitumor and antimicrobial properties in various studies.
  • Due to the presence of multiple functional groups, this compound can be utilized in the synthesis of other complex organic molecules, thus serving as a valuable intermediate in organic synthesis.

In summary, 1-anilino-3-phenylimino-urea exemplifies the connection between simple chemical structures and their potential in significant applications ranging from industrial to pharmaceutical uses. As we delve deeper into the chemistry of such compounds, we unlock new possibilities for innovation and discovery.

Synonyms
Diphenylcarbazone
1,5-Diphenylcarbazone
Diazenecarboxylic acid, phenyl-, 2-phenylhydrazide
Phenylazoformic acid 2-phenylhydrazide
Diphenylcarbazone [MI]
Diphenylcarbazone, (E)-
Diphenylcarbazone (E)-form
sym-Diphenylcarbazone
EINECS 208-698-0
BRN 0959475
119295-41-9
3-Hydroxy-1,5-diphenylformazan
UNII-96YS88318X
Phenyldiazenecarboxylic acid 2-phenylhydrazide
96YS88318X
(Phenylazo)formic acid 2-phenylhydrazide
FORMIC ACID, (PHENYLAZO)-, 2-PHENYLHYDRAZIDE
Diazenecarboxylic acid, phenyl-, 2-phenylhydrazide, (1E)-
DTXSID5060225
4-16-00-00017 (Beilstein Handbook Reference)
Diazenecarboxylic acid, 2-phenyl-, 2-phenylhydrazide
Diazenecarbohydrazonic acid, N,2-diphenyl-
Hydrazinecarboxamide, 2-phenyl-N-(phenylimino)-
sDiphenylcarbazone
1,5Diphenylcarbazone
DTXCID6041509
(Phenylazo)formic acid 2phenylhydrazide
Formic acid, (phenylazo), 2phenylhydrazide
Phenyldiazenecarboxylic acid 2phenylhydrazide
Diazenecarboxylic acid, 2phenyl, 2phenylhydrazide
Diazenecarboxylic acid, phenyl, 2phenylhydrazide
zfwahzcokgwuit-bmradrmjsa-n
538-62-5
1-anilino-3-phenyliminourea
(E)-1,5-Diphenylcarbazone
Diphenylcarbazone, (Z)-
5UYJ4R0D5T
CHEMBL79409
(E)-N',2-Diphenyldiazenecarbohydrazide
Diazenecarboxylic acid, phenyl-, 2-phenylhydrazide, (Z)-
119295-40-8
UNII-5UYJ4R0D5T
diphenylcarbazon
1,5-Diphenylcarbazone Compound With 1,5-Diphenylcarbazide (Technical Grade)
MFCD00003024
(Z)-diphenylcarbazone
Diphenylcarbazone, p.a.
carbazone, 1,5-diphenyl-
SCHEMBL1057265
SCHEMBL1551533
ZFWAHZCOKGWUIT-UHFFFAOYSA-N
N',2-diphenyldiazenecarbohydrazide
BDBM50071644
N',2-Diphenyldiazenecarbohydrazide #
STL280245
DIPHENYLCARBAZONE Z-FORM [MI]
AKOS003273042
AKOS024348870
FD32398
(E)-N'',2-diphenyldiazenecarbohydrazide
(E)-1-(phenylamino)-3-(phenylimino)urea
CS-0132463
D0881
NS00032860
1,5-Diphenylcarbazone (for colorimetry tests)
Diphenylcarbazone (contains Diphenylcarbazide)
H11948
AA-516/30131025
Q1227136
Q27262902
Q27271938