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C24H13Cl3N2O4

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Identification
Molecular formula
C24H13Cl3N2O4
CAS number
21213-43-6
IUPAC name
4-(dimethylamino)-N-[7-(hydroxyamino)-7-oxo-heptyl]benzamide
State
State

This compound appears in a solid state under standard conditions (25°C and 1 atm). It is typically found as a powder or in a crystalline form due to its stable molecular structure.

Melting point (Celsius)
218.50
Melting point (Kelvin)
491.65
Boiling point (Celsius)
458.20
Boiling point (Kelvin)
731.35
General information
Molecular weight
443.63g/mol
Molar mass
443.6270g/mol
Density
1.8312g/cm3
Appearence

This chemical is typically presented as a colorless to white crystalline powder. Due to its chemical structure, it may exhibit different physical states depending on processing and purification methods.

Comment on solubility

Solubility of 4-(dimethylamino)-N-[7-(hydroxyamino)-7-oxo-heptyl]benzamide

The solubility of 4-(dimethylamino)-N-[7-(hydroxyamino)-7-oxo-heptyl]benzamide, with the chemical formula C24H13Cl3N2O4, can be quite intriguing due to its complex molecular structure. The solubility characteristics can be summarized as follows:

  • Polarity: The presence of the hydroxyamino and dimethylamino groups suggests some level of polarity, which may enhance its solubility in polar solvents such as water or alcohols.
  • Hydrophilic vs. Hydrophobic: The molecule exhibits both hydrophilic and hydrophobic characteristics, meaning that it may have varying solubility in different environments.
  • Solvent Compatibility: In organic solvents, solubility may be higher due to the non-polar aspects of the hydrocarbon chains. However, in water, solubility might be limited due to the bulky nature of the aromatic and aliphatic components.

In practical terms, one might observe:

  • High solubility in polar organic solvents
  • Moderate solubility in water
  • Efforts to modify the compound through derivatization could influence solubility behavior significantly.

In conclusion, understanding the solubility of this compound is crucial for its applications, as it determines the most suitable solvent for use in various chemical processes. As the saying goes, "Like dissolves like," highlighting the importance of considering both medicinal and industrial uses when assessing solubility.

Interesting facts

Interesting Facts about 4-(Dimethylamino)-N-[7-(hydroxyamino)-7-oxo-heptyl]benzamide

This intriguing compound is known for its complex structure and potential applications in various fields of chemistry and medicine. Here are some noteworthy aspects:

  • Structure and Functionality: The compound features a benzamide core, which is a common structure in many pharmaceutical agents. Its unique side chains, especially the hydroxyamino and oxo groups, contribute to its distinct chemical behavior.
  • Potential in Medicinal Chemistry: Compounds with amino and hydroxy functionalities are often investigated for their biological activity. This compound may serve as a lead in drug discovery, particularly for targeting specific enzymes or receptors in the body.
  • Research Applications: The presence of dimethylamino groups can enhance lipophilicity, potentially improving the compound's ability to penetrate cell membranes. This characteristic makes it a candidate for studies in drug delivery systems.
  • Environmental Considerations: Understanding how such complex compounds behave in biological and environmental systems is crucial. Research can help elucidate their degradation pathways and fate in ecosystems, ensuring safety and efficacy in proposed applications.
  • In Silico Studies: Computational chemistry techniques can be employed to predict the reactivity and interaction of this compound with various pharmacological targets. These studies can guide experimental designs and optimize drug development processes.

In summary, 4-(dimethylamino)-N-[7-(hydroxyamino)-7-oxo-heptyl]benzamide not only captivates the interest of chemists and biologists alike but also promises exciting avenues for research and application in the realm of medicinal chemistry. Its intricate structure and chemical properties underscore the importance of interdisciplinary approaches in modern scientific inquiries.

Synonyms
251456-60-7
m344
4-(dimethylamino)-n-[7-(hydroxyamino)-7-oxoheptyl]benzamide
M 344
Histone Deacetylase Inhibitor III
4-(dimethylamino)-N-(7-(hydroxyamino)-7-oxoheptyl)benzamide
N-Hydroxy-7-(4-dimethylaminobenzoyl)aminoheptanamide
M-344
Benzamide, 4-(dimethylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]-
4-Dimethylamino-N-(6-hydroxycarbamoylhexyl)benzamide
MFCD03453554
J8W4VF5ZEJ
D 237;MS 344
CHEMBL140000
4-DIMETHYLAMINO-N-(6-HYDROXYCARBAMOYLHEXYL)-BENZAMIDE
CHEBI:125562
N-Hydroxy-7-(4-dimethylaminobenzoyl)-aminoheptanamide
4-(Dimethylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]-benzamide
7-{[4-(DIMETHYLAMINO)PHENYL]FORMAMIDO}-N-HYDROXYHEPTANAMIDE
Benzamide, 4-(dimethylamino)-N-(7-(hydroxyamino)-7-oxoheptyl)-
7-((4-(dimethylamino)phenyl)formamido)-N-hydroxyheptanamide
B3N
MS 344, D237
UNII-J8W4VF5ZEJ
MLS006011092
SCHEMBL675763
4-(dimethylamino)-NHAOBzNH2
DTXSID90274415
GLXC-02057
HMS3648E20
HMS3656B08
M344 (GMP)
BDBM50082665
HY-13506G
NSC718169
s2779
AKOS022183358
CCG-208693
CS-1342
DB02565
NSC-718169
M344, >=98% (HPLC), powder
NCGC00263617-05
AS-71316
D237
HY-13506
NCI60_040738
SMR004702880
DB-106167
D4188
NS00070625
SW219379-1
N-6-Hydroxamohexyl-4-(dimethylamino)benzamide
C74302
M 344?
SR-01000946361
SR-01000946361-1
BRD-K45528773-001-02-3
BRD-K45528773-001-03-1
BRD-K45528773-001-06-4
BRD-K45528773-001-07-2
Q27216175
4-Dimethylamino-N-(6-hydroxycarbamoyl-hexyl)-benzamide