CAS 88519-57-7
:N-(4-aminobutyl)-5-chloro-2-*naphthalenesulfonami
Description:
N-(4-aminobutyl)-5-chloro-2-naphthalenesulfonamide, with the CAS number 88519-57-7, is a chemical compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. This compound features a naphthalene ring system, which contributes to its aromatic stability and potential interactions in biological systems. The presence of the amino group (–NH2) and the chloro substituent (–Cl) on the naphthalene structure may influence its reactivity and solubility in various solvents. Typically, sulfonamides exhibit moderate to high solubility in polar solvents due to their ability to form hydrogen bonds. The compound may also demonstrate biological activity, potentially acting as an inhibitor or modulator in various biochemical pathways. Its structural characteristics suggest potential applications in pharmaceuticals or as a research tool in medicinal chemistry. However, specific biological activities, toxicity, and environmental impact would require further investigation through empirical studies.
Formula:C14H18Cl2N2O2S
InChI:InChI=1/C14H17ClN2O2S.ClH/c15-14-5-3-4-11-10-12(6-7-13(11)14)20(18,19)17-9-2-1-8-16;/h3-7,10,17H,1-2,8-9,16H2;1H
SMILES:C(CCNS(=O)(=O)c1ccc2c(cccc2Cl)c1)CN.Cl
Synonyms:- W-13, HCl
- N-(4-Aminobutyl)-5-Chloro-2-Naphthalenesulfonamide, Hydrochloride
- N-(4-aminobutyl)-5-chloronaphthalene-2-sulfonamide hydrochloride (1:1)
- W-13 HYDROCHLORIDE
- N-(4-AMINOBUTYL)-5-CHLORO-2-NAPHTHALENESULFONAMIDE HCL
- W-13, Hydrochloride - CAS 88519-57-7 - Calbiochem
- N
- W-13
- N-(4-AMINOBUTYL)-5-CHLORO-2- &
- N-(4-Aminobutyl)-5-chloronaphthalene-2-sulfonamide Hydrochloride >
- N-(4-Aminobutyl)-5-chloronaphthalene-2-sulphonamide hydrochloride
- OMEGA-13 HYDROCHLORIDE
- 4-[(5-chloro-2-naphthalenyl)sulfonylamino]butylammonium
- N-(4-Aminohexyl)-5-chloro-2-naphthalenesulfonamide hydrochloride
- (+)-5-Hydroxy-8-[5-(5-hydroxy-7-methoxy-4-oxo-4H-1-benzopyran-2-yl)-2-methoxyphenyl]-7-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
- N-(4-AMinobutyl)-5-chloro-2-naphthalenesulfonaMide Monohydrochloride
- N-(4-aminobutyl)-5-chloro-2-*naphthalenesulfonami
- N-(4-AMinobutyl)-5-chloronaphthalene-2-sulfonaMide Hydrochloride
- W-13 HYDROCHLORIDE CALMODULIN ANTAGONIST
- N-(4-AMINOBUTYL)-5-CHLORO-2-NAPHTHALENE SULPHONAMIDE, HYDROCHLORIDE
- -(4-Aminobutyl)-5-chloronaphthalene-2-sulfonamide Hydrochloride
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Found 7 products.
2-Naphthalenesulfonamide, N-(4-aminobutyl)-5-chloro-, hydrochloride (1:1)
CAS:Formula:C14H18Cl2N2O2SPurity:95%Color and Shape:SolidMolecular weight:349.2759N-(4-Aminobutyl)-5-chloronaphthalene-2-sulphonamide hydrochloride
CAS:N-(4-Aminobutyl)-5-chloronaphthalene-2-sulphonamide hydrochlorideFormula:C14H17ClN2O2S·ClHPurity:≥98%Molecular weight:349.27592N-(4-Aminobutyl)-5-chloronaphthalene-2-sulfonamide Hydrochloride
CAS:Formula:C14H17ClN2O2S·HClPurity:>98.0%(HPLC)(N)Color and Shape:Light orange to Light red powder to crystallineMolecular weight:349.27W-13 HCl
CAS:N-(4-Aminobutyl)-5-chloronaphthalene-2-sulfonamide hydrochlorideFormula:C14H18Cl2N2O2SPurity:95%Molecular weight:349.28N-(4-Aminobutyl)-5-chloro-2-naphthalenesulfonamide Hydrochloride
CAS:Controlled ProductApplications Calmodulin antagonist that binds to calmodulin and inhibits calcium-ion-calmodulin- regulated activities, including phosphodiesterase activation and myosin light chain kinase.
References Hidaka, H., et al.: Protein, Nuc. Acid and Enzyme, 26, 977 (1981), Hidaka, H., et al.: Mol. Pharm., 20, 571 (1981), Inagaki, et al.: Pharmacology, 27, 125 (1983)Formula:C14H17ClN2O2S·ClHColor and Shape:NeatMolecular weight:349.28W-13 hydrochloride
CAS:W-13 hydrochloride (W-13 HCl) is a calmodulin antagonist.Formula:C14H18Cl2N2O2SPurity:98.51%Color and Shape:SolidMolecular weight:349.28
