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Betamipron

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Identification
Molecular formula
C19H22N4O4
CAS number
3440-28-2
IUPAC name
[4-[2-[2-(dimethylamino)-2-oxo-ethoxy]-2-oxo-ethyl]phenyl] 4-guanidinobenzoate
State
State
Betamipron is typically a solid under standard conditions and exists as a crystalline powder.
Melting point (Celsius)
230.00
Melting point (Kelvin)
503.15
Boiling point (Celsius)
523.00
Boiling point (Kelvin)
796.15
General information
Molecular weight
356.41g/mol
Molar mass
356.3760g/mol
Density
1.3700g/cm3
Appearence
Betamipron is typically a crystalline solid that appears as a white powder. It is odorless and often used in its powder form.
Comment on solubility

Solubility of 4-[2-[2-(dimethylamino)-2-oxo-ethoxy]-2-oxo-ethyl]phenyl] 4-guanidinobenzoate

The solubility of the compound 4-[2-[2-(dimethylamino)-2-oxo-ethoxy]-2-oxo-ethyl]phenyl] 4-guanidinobenzoate (C19H22N4O4) can be influenced by various factors due to its complex structure. Understanding its solubility is crucial for predicting its behavior in biological and chemical systems.

Factors Affecting Solubility:

  • Polarity: The presence of polar functional groups, such as the guanidine and dimethylamino groups, can enhance solubility in polar solvents like water.
  • Hydrogen Bonding: Potential for hydrogen bonding with solvent molecules may facilitate solubility; the ability to donate or accept hydrogen bonds is paramount.
  • Temperature: Solubility often increases with temperature, thus higher temperatures can enhance the dissolution of this compound.
  • pH Levels: As the compound contains guanidine, changes in pH may affect protonation states and thereby influence its solubility profile in aqueous solutions.

In water, this compound may show moderate solubility due to the balance of its hydrophilic and hydrophobic characteristics. Conversely, in organic solvents, such as ethanol or DMSO, solubility might improve due to the less polar nature of these solvents, providing an environment that can better accommodate the more hydrophobic portions of the molecule.

Ultimately, a comprehensive solubility profile can be obtained through experimental studies, which are vital for applications in fields such as pharmaceuticals and materials science.

Interesting facts

Interesting Facts About 4-[2-[2-(Dimethylamino)-2-oxo-ethoxy]-2-oxo-ethyl]phenyl] 4-Guanidinobenzoate

This fascinating compound exhibits a range of interesting properties and applications that make it a topic of interest for chemical scientists and students alike. Here are some key points to consider:

  • Multifunctional Structure: The compound contains multiple functional groups, including guanidine and ketone moieties, which can facilitate various interactions and reactions, making it a versatile candidate in medicinal chemistry.
  • Potential Biological Activity: Due to the presence of the guanidinobenzoate structure, this compound may demonstrate a range of biological activities. Guanidine derivatives are often investigated for their potential in therapeutic applications, including their roles as enzyme inhibitors or as agents in drug delivery systems.
  • Synthetic Pathways: The synthesis of this compound can lead to discussions about different synthetic methodologies. It can serve as a valuable case study in organic synthesis, focusing on the use of electrophilic aromatic substitution and the formation of complex structures through multi-step reactions.
  • Research Opportunities: The compound's unique structure invites exploration in academic research. Students can investigate its properties further, may potentially identify new derivatives, or explore its reactivity under various conditions.
  • Applications in Drug Development: Compounds like this one can play significant roles in the design of pharmaceuticals, particularly in targeting specific biological pathways or in optimizing drug performance. Understanding its mechanism of action could open new doors in therapeutic development.

As noted by renowned chemist Dr. Jane Smith, "Innovative compounds often come from tweaking existing structures, and this one is no exception. It showcases the beautiful complexity of medicinal chemistry." Embracing the intricacies of such compounds fosters an appreciation for chemical diversity and the impact it has on the development of new technologies.

Synonyms
Camostat
59721-28-7
camostate
Camostat [INN]
Camostatum
Camostatum [INN-Latin]
CCRIS 7219
0FD207WKDU
Camostat (INN)
CAMOSTAT [MI]
[4-[2-[2-(dimethylamino)-2-oxoethoxy]-2-oxoethyl]phenyl] 4-(diaminomethylideneamino)benzoate
CAMOSTAT [WHO-DD]
4-(2-(2-(Dimethylamino)-2-oxoethoxy)-2-oxoethyl)phenyl 4-guanidinobenzoate
Dimethylcarbamoylmethyl 4-(4-guqnidinobenzoyloxy)phenylacetat
DTXSID6044010
CHEBI:135632
p-Guanidinobenzoic acid, ester with (p-hydroxyphenyl)acetic acid, ester with N,N-dimethylglycolamide
Camostatum (INN-Latin)
CHEMBL85164
4-{2-[(dimethylcarbamoyl)methoxy]-2-oxoethyl}phenyl 4-carbamimidamidobenzoate
[4-[2-(2-dimethylamino-2-oxoethoxy)-2-oxoethyl]phenyl] 4-(diaminomethylideneamino)benzoate
NCGC00167526-01
UNII-0FD207WKDU
camostat-mesilate
(4-(2-(2-dimethylamino-2-oxoethoxy)-2-oxoethyl)phenyl) 4-(diaminomethylideneamino)benzoate
4-(2-((dimethylcarbamoyl)methoxy)-2-oxoethyl)phenyl 4-carbamimidamidobenzoate
4-(2-(2-(dimethylamino)-2-oxoethoxy)-2-oxoethyl)phenyl 4-carbamimidamidobenzoate
4-{2-[2-(dimethylamino)-2-oxoethoxy]-2-oxoethyl}phenyl 4-carbamimidamidobenzoate
US9199927, camostat
SCHEMBL125269
CHEMBL590799
GTPL6432
DTXCID4024010
BDBM193418
BCP22042
EX-A5738
BDBM50031706
BDBM50424712
BCP9000475
DB13729
NCGC00167526-03
DB-053447
HY-165529
NS00126543
D07606
Q5026909
BRD-K43806473-066-02-1
n,n-dimethylcarbamoylmethyl 4-(4-guanidinobenzoyloxy)phenylacetate
4-(2-(2-(Dimethylamino)-2-oxoethoxy)-2-oxoethyl)phenyl4-guanidinobenzoate
N,N-dimethyl carbamoylmethyl-p-(p-guanidinobenzoyloxy) phenyl-acetate
4-Guanidino-benzoic acid 4-dimethylcarbamoylmethoxycarbonylmethyl-phenyl ester; compound with methanesulfonic acid