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Fluorescein amine

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Identification
Molecular formula
C14H17ClN2O2S
CAS number
37628-68-3
IUPAC name
N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide
State
State

At room temperature, N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide exists as a solid. It is stable under standard conditions but should be stored in a cool, dry place to maintain its integrity.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
297.80g/mol
Molar mass
297.8040g/mol
Density
1.2000g/cm3
Appearence

The compound typically appears as a light yellow powder or crystalline solid. Its appearance may vary slightly depending on its purity and specific processing methods. In solution, depending on the concentration and solvent used, it could exhibit a light yellow color.

Comment on solubility

Solubility of N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide

The solubility of the compound N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide (C14H17ClN2O2S) can provide crucial insights into its potential applications and behavior in various environments. Here are some key points regarding its solubility:

  • Polar vs. Non-polar: The presence of functional groups, such as the sulfonamide group, suggests some degree of polarity. This typically enhances solubility in polar solvents, such as water.
  • Solvent Specificity: It is expected to be more soluble in organic solvents due to its hydrophobic naphthalene structure, which may limit its solubility in water.
  • Temperature Dependency: Like many organic compounds, solubility may increase with temperature, facilitating dissolved concentrations.
  • pH Influence: Being a sulfonamide, its solubility might also be influenced by pH, potentially altering the ionization state of the molecule and affecting its solubility profile.

In conclusion, while its chemical structure indicates potential polar interactions, the presence of hydrophobic elements suggests a complex solubility behavior; as such, it may exhibit variable solubility characteristics depending on the solvent and environmental conditions. Understanding these factors can be vital for both practical applications and for predicting behavior in biochemical systems.

Interesting facts

Interesting Facts about N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide

N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide, often referred to as a chlorinated sulfonamide compound, possesses several remarkable characteristics and applications that pique the interest of chemists and researchers alike.

Key Highlights

  • Antimicrobial Properties: This compound falls under the broader category of sulfonamides, which have long been recognized for their antibacterial activity. The development of sulfonamides revolutionized modern medicine in the early 20th century as some of the first effective antibiotics.
  • Structural Significance: The naphthalene ring system adds notable stability and can influence the biological activity of the compound, given its ability to interact with various biological targets.
  • Applications: Beyond its medicinal uses, the compound’s unique structure opens doors to potential applications in other fields such as materials science and agrochemicals. Its reactivity may lead to synthesis pathways for other important compounds.
  • Research Potential: As ongoing studies continue to unveil the multifaceted roles of sulfonamide derivatives, N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide presents a promising candidate for investigations into new therapeutic agents.

The process of synthesizing and studying this compound can be particularly intriguing due to its chiral centers and specific binding interactions, capturing the attention of both organic chemists and those interested in pharmacology.

Moreover, if you're keen on exploring the chemistry behind this compound, consider examining its mechanisms of action, which may include inhibition of bacterial folic acid synthesis, a significant metabolic pathway in many microorganisms. One notable quote in the field states, “The structure of a compound often dictates its function,” highlighting the importance of understanding compounds like N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide in the context of their therapeutic uses.

In conclusion, N-(4-aminobutyl)-5-chloro-naphthalene-2-sulfonamide serves as a testament to the intersection of structure, function, and application in chemistry, making it a fascinating subject for both current and future research pursuits.

Synonyms
N-(4-aminobutyl)-5-chloronaphthalene-2-sulfonamide
w-13
N-(4-Aminobutyl)-5-Chloro-2-Naphthalenesulfonamide
CHEBI:75366
2-Naphthalenesulfonamide, N-(4-aminobutyl)-5-chloro-
Tocris-0361
SCHEMBL905271
CHEMBL1256392
DTXSID401002136
HMS3742E03
HSCI1_000322
NCGC00024554-01
BRD-K45068323-003-01-3
BRD-K45068323-003-02-1
N-(4-aminobutyl)-5-chloro-2-naphthalene sulfonamide
Q27145252