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JNK Inhibitor II

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Identification
Molecular formula
C16H22N2O2S
CAS number
1866-31-5
IUPAC name
N-(6-aminohexyl)naphthalene-1-sulfonamide
State
State

At room temperature, N-(6-aminohexyl)naphthalene-1-sulfonamide is solid.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
405.00
Boiling point (Kelvin)
678.15
General information
Molecular weight
306.43g/mol
Molar mass
306.4260g/mol
Density
1.2870g/cm3
Appearence

N-(6-aminohexyl)naphthalene-1-sulfonamide appears as a white to off-white powder or solid.

Comment on solubility

Solubility of N-(6-aminohexyl)naphthalene-1-sulfonamide

N-(6-aminohexyl)naphthalene-1-sulfonamide, with the chemical formula C16H22N2O2S, exhibits notable solubility characteristics that are essential for its applications in various chemical contexts. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is likely to have varied solubility in organic solvents due to the presence of the hydrophobic naphthalene moiety 1 and the more polar sulfonamide group 2.
  • Water Solubility: The presence of sulfonamide suggests that it may have some degree of solubility in water, although the hydrophobic sections may limit this.
  • Polar vs. Non-Polar Solvents: It can be anticipated that non-polar solvents might dissolve the compound more effectively than polar solvents, based on its structural components.
  • Temperature Influence: Like many organic compounds, its solubility may increase with temperature, making higher temperatures advantageous for dissolution.

The solubility behavior of N-(6-aminohexyl)naphthalene-1-sulfonamide indicates how the properties of individual molecular groups can influence the overall interaction with solvents, leading to essential applications in chemical synthesis and formulation.

Please refer to specific solubility studies for quantitative data and further insights.

Interesting facts

Interesting Facts about N-(6-aminohexyl)naphthalene-1-sulfonamide

N-(6-aminohexyl)naphthalene-1-sulfonamide, often known for its unique structure and functional properties, is a compound that stands out in the world of chemistry. Here are some engaging insights:

  • Structure and Functionality: This compound features a naphthalene ring, which is significant for its stability and aromatic characteristics. The sulfonamide group adds to its reactivity, making it a valuable candidate in various chemical reactions.
  • Biological Relevance: Sulfonamides are historically prominent in the field of medicinal chemistry, especially as antimicrobial agents. Their ability to inhibit bacterial growth marks them as critical in the development of pharmaceuticals.
  • Applications: Beyond its medicinal uses, this compound may also find applications in materials science and organic synthesis, particularly due to the naphthalene moiety, which can participate in various chemical transformations.
  • Development of New Compounds: The synthesis of such sulfonamide derivatives can often lead to novel compounds with enhanced biological activities or specific functionalities that could be beneficial in drug design.

As quoted from renowned chemist Sir Derek Barton, "The most important thing for the chemist is not the atoms themselves but the way they are arranged." The arrangement in N-(6-aminohexyl)naphthalene-1-sulfonamide indeed illustrates this principle, showcasing how structure influences function significantly.

Understanding this compound not only enriches our knowledge of sulfonamides but also exemplifies the intricate relationship between molecular structure and chemical properties, paving the way for innovative research in various scientific fields.

Synonyms
N-(6-aminohexyl)naphthalene-1-sulfonamide
N-(6-Aminohexyl)-1-Naphthalenesulfonamide
79458-81-4
UNII-7B979CWO03
7B979CWO03
1-Naphthalenesulfonamide, N-(6-aminohexyl)-
AMINOHEXYL)-1-NAPTHALENESULFONAMIDE, N-(6-
Tocris-0368
naphthalene-1-sulfonic acid (6-aminohexyl)-amide
SCHEMBL413671
CHEMBL1188431
CHEBI:92739
FVJRBJIENDRNBE-UHFFFAOYSA-N
DTXSID301000494
KUC110440N
HSCI1_000203
KSC-210-108
NCGC00024556-01
NCGC00024556-02
W 5
DB-352400
naphthalene-1-sulfonic acid (6-amino-hexyl)-amide
BRD-K41868777-003-01-1
BRD-K41868777-003-02-9
Q27164504