Skip to main content

AMPPNP

ADVERTISEMENT
Identification
Molecular formula
C19H22N6O
CAS number
962961-93-5
IUPAC name
1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea
State
State

This compound is typically found as a solid at room temperature. It is stable under standard storage conditions and should be handled to prevent contact with skin and eyes.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.00
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.00
General information
Molecular weight
358.43g/mol
Molar mass
358.4260g/mol
Density
1.4000g/cm3
Appearence

1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea typically appears as a white crystalline solid. It is often provided as a powder or in crystalline form.

Comment on solubility

Solubility of 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea

1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea, a complex organic compound, exhibits intriguing solubility characteristics that are worth noting. Its solubility is influenced by several factors:

  • Polarity: The presence of urea functional groups contributes to its moderate polarity, which can enhance solubility in polar solvents.
  • Solvent Interaction: This compound is typically more soluble in polar protic solvents such as water or alcohols due to hydrogen bonding.
  • Temperature Effects: Higher temperatures may improve solubility by overcoming molecular interactions that could hinder dissolution.
  • pH Considerations: The solubility may also vary with pH, as changes in the protonation state of imidazole rings can significantly affect solubility in aqueous solutions.

In summary, while 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea demonstrates reasonable solubility in various solvents, it is primarily dependent on the solvent's nature and the environmental conditions. To gain a comprehensive understanding of its solubility profile, extensive experimental data is valuable. As a result, it's crucial to consult specific solubility studies or experimental conditions that can provide insight into its solvent capabilities.

Interesting facts

Interesting Facts about 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea

This compound, known as 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea, belongs to a class of compounds that are gaining attention in the field of medicinal chemistry due to their potential biological activities. Here are some fascinating highlights:

  • Diverse Biological Activities: Compounds like this one exhibit a range of biological properties, including antitumor and antibacterial effects. This makes them valuable in the search for new therapeutic agents.
  • Urea Moiety: The presence of the urea functional group is notable, as it plays a pivotal role in the biological activity of many pharmaceuticals. Urea derivatives can engage in strong hydrogen bonding interactions, enhancing their efficacy.
  • Imidazole Ring: The incorporation of the 4,5-dihydro-1H-imidazol-2-yl moiety contributes to the compound's biological profile. Imidazoles are commonly found in numerous bioactive molecules and are known for their role in enzyme inhibition.
  • Structural Complexity: The compound showcases a significant structural complexity with multiple aromatic rings, which can lead to interesting electronic properties, offering exciting pathways for further research.
  • Research Potential: Ongoing research may unlock new applications in chemical biology. Investigators are eager to explore its mechanism of action, potentially leading to groundbreaking treatments for various diseases.

As scientists continue to unravel the mysteries of compounds like this, it’s clear that their unique structures and diverse biological activities could pave the way for innovative therapies in the future. “The exploration of such compounds is not just a journey into chemistry but also into the future of medicine.”

Synonyms
Imidocarb
27885-92-3
1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea
Imidocarbe
Imidocarbo
Imidocarbum
1,3-Bis(3-(2-imidazolin-2-yl)phenyl)urea
N,N'-Bis(3-(4,5-dihydro-1H-imidazol-2-yl)phenyl)urea
1,3-Bis(3-(2-imidazolin-2-yl)phenyl)harnstoff
UNII-8USS3K0VDH
Imidocarbe [INN-French]
Imidocarbum [INN-Latin]
8USS3K0VDH
Imidocarbo [INN-Spanish]
EINECS 248-711-7
BRN 0964732
Urea, N,N'-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]-
CARBANILIDE, 3,3'-DI-2-IMIDAZOLIN-2-YL-
CHEBI:51804
3,3'-Di-2-imidazolin-2-ylcarbanilide
1,3-bis(3-(4,5-dihydro-1H-imidazol-2-yl)phenyl)urea
DTXSID0048345
Urea, N,N'-bis(3-(4,5-dihydro-1H-imidazol-2-yl)phenyl)-
5-25-11-00011 (Beilstein Handbook Reference)
Imidocarbe (INN-French)
Imidocarbum (INN-Latin)
Imidocarbo (INN-Spanish)
IMIDOCARB (MART.)
IMIDOCARB [MART.]
N,N'-Bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea
Imizol (veterinary)
DTXCID5028320
248-711-7
TCMDC-124304
CHEMBL427342
Imidocarb (INN)
IMIDOCARB [INN]
Imidocarb [INN:BAN]
MLS001336005
NSC51189
Imidocarb 100 microg/mL in Methanol
SMR000875323
MFCD00693581
Imizad (dipropionate)
Imizol (dipropionate)
1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea;propanoic acid
IMIDOCARB [MI]
4A65 (dihydrochloride)
Imizocarb (dihydrochloride)
Imizol [veterinary] (TN)
TimTec1_002508
SCHEMBL203921
cid_114961
BDBM79241
HMS1541B22
KUC108633N
BCP22333
Imidocarbum; Imidocarbe; Imidocarbo
FD7211
MMV665810
NSC766768
STK379516
AKOS005449571
1ST7182
DB11521
KS-5199
KSC-19-203
NSC-766768
NCGC00174046-01
DB-014824
HY-135611
CS-0113606
NS00000020
D08069
EN300-7357087
Q908851
1,3-bis[3-(2-imidazolin-2-yl)phenyl]urea;propionic acid
N,N'-Bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea #