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ML-7

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Identification
Molecular formula
C16H21ClN2O2S
CAS number
110448-33-4
IUPAC name
N-(6-aminohexyl)-5-chloro-naphthalene-1-sulfonamide
State
State

ML-7 is typically found as a solid at room temperature.

Melting point (Celsius)
207.00
Melting point (Kelvin)
480.15
Boiling point (Celsius)
524.00
Boiling point (Kelvin)
797.15
General information
Molecular weight
376.88g/mol
Molar mass
376.8870g/mol
Density
1.3500g/cm3
Appearence

ML-7 is typically a white or off-white solid powder. It is crystalline in nature and can be partially soluble in some organic solvents.

Comment on solubility

Solubility of N-(6-aminohexyl)-5-chloro-naphthalene-1-sulfonamide (C16H21ClN2O2S)

The solubility of N-(6-aminohexyl)-5-chloro-naphthalene-1-sulfonamide can be influenced by a variety of factors due to its complex molecular structure. Generally, the solubility behavior of this compound can be summarized as follows:

  • Polarity: The presence of the sulfonamide group (–SO2NH2) in the molecular structure suggests potential for polar interactions. This typically enhances solubility in polar solvents like water.
  • Hydrophobic Character: The naphthalene ring and alkyl chain impart a greater hydrophobic character, which may limit solubility in polar solvents but could enhance solubility in organic solvents such as ethanol or acetone.
  • Temperature Influence: Solubility may increase with temperature as kinetic energy promotes solvent-solute interactions, making it easier for the solute to disperse.
  • pH Dependence: As a sulfonamide, the compound's solubility can also depend on the pH of the solution, where ionization can enhance solubility in more alkaline environments.

In practice, this compound may exhibit variable solubility characteristics depending on the solvent and environmental conditions. Therefore, experimental determination of solubility under various conditions is recommended for precise applications.

Interesting facts

Interesting Facts About N-(6-Aminohexyl)-5-chloro-naphthalene-1-sulfonamide

N-(6-Aminohexyl)-5-chloro-naphthalene-1-sulfonamide is an intriguing compound with a variety of chemical properties and potential applications. Here are some fascinating aspects of this compound:

  • Pharmaceutical Relevance: This compound is part of a class of sulfonamides that have been extensively studied for their antimicrobial properties. Its structure suggests potential efficacy against various bacterial infections.
  • Versatile Chemistry: The presence of both an amino group and a sulfonyl group in its structure allows for diverse chemical reactivity. This versatility can lead to significant implications in drug development.
  • Structure-Activity Relationship (SAR): The specific arrangement of functional groups contributes to the compound's biological activity. Researchers often focus on SAR to modify compounds to enhance their effectiveness while reducing side effects.
  • Environmental Science: This compound may be researched for its behavior in environmental contexts, particularly regarding its stability and degradation pathways, as sulfonamide antibiotics can impact ecosystems.
  • Potential Industrial Applications: Beyond medicinal uses, N-(6-aminohexyl)-5-chloro-naphthalene-1-sulfonamide may find roles in the development of inhibitors in chemical processes, showcasing its multifunctional capabilities.

As a compound at the intersection of organic chemistry and pharmacology, N-(6-aminohexyl)-5-chloro-naphthalene-1-sulfonamide illustrates the complexity and potential of chemical research. Scientists continue to explore its properties, aiming to unlock further therapeutic applications and improve our understanding of sulfonamides.

Synonyms
N-(6-AMINOHEXYL)-5-CHLORO-1-NAPHTHALENESULFONAMIDE
65595-90-6
N-(6-aminohexyl)-5-chloronaphthalene-1-sulfonamide
1-NAPHTHALENESULFONAMIDE, N-(6-AMINOHEXYL)-5-CHLORO-
W 7
CHEMBL41631
N-AMINOHEXYL-5-CHLORO-1-NAPTHALENESULFONAMIDE HYDROCHLORIDE
W7
N-(6-Aminohexyl)-5-chloro-1-naphthalenesulphonamide
Spectrum_000286
BRN 2888957
Spectrum_001450
Tocris-0369
starbld0016247
Spectrum2_001569
Spectrum3_001600
Spectrum4_000316
Spectrum5_001878
Lopac-A-3281
Lopac0_000075
BSPBio_001230
BSPBio_003200
KBioGR_000932
KBioSS_000766
KBioSS_001930
DivK1c_000102
DivK1c_000129
DivK1c_001015
SCHEMBL166960
SPBio_001478
HMS500F04
KBio1_000102
KBio1_000129
KBio1_001015
KBio2_000766
KBio2_001930
KBio2_003334
KBio2_004498
KBio2_005902
KBio2_007066
KBio3_002700
DTXSID80984172
IDEHCMNLNCJQST-UHFFFAOYSA-N
NINDS_000102
NINDS_000129
NINDS_001015
Bio1_000399
Bio1_000888
Bio1_001377
KUC109782N
BDBM50111446
CA-320
AKOS040754388
CCG-204170
DB04513
IDI1_000102
IDI1_000129
IDI1_001015
KSC-210-030
NCGC00015050-01
NCGC00015050-02
NCGC00015050-03
NCGC00015050-04
NCGC00015050-05
NCGC00024557-01
NCGC00024557-02
NCGC00024557-03
NS00011713
N-(6-Aminohexyl)-1-chloronaphthalene-5-sulfonamide
N-AMINOHEXYL-5-CHLORONAPHTH-1-YLSULFONAMIDE
Q2536561
BRD-K90259198-003-02-2
BRD-K90259198-003-04-8
[6-[[(5-Chloronaphthalen-1-yl)sulfonyl]amino]hexyl]amine
5-Chloro-naphthalene-1-sulfonic acid (6-amino-hexyl)-amide