N-(4-aminobutyl)-5-chloro-2-naphthalenesulfonamide hydrochloride

Suppliers

Names

[ CAS No. ]:
88519-57-7

[ Name ]:
N-(4-aminobutyl)-5-chloro-2-naphthalenesulfonamide hydrochloride

[Synonym ]:
N-(4-Aminobutyl)-5-chloronaphthalene-2-sulfonamide hydrochloride (1:1)
MFCD00058030
W-13,Hydrochloride
N-(4-Aminobutyl)-5-chloro-2-naphthalenesulfonamide hydrochloride (1:1)
2-Naphthalenesulfonamide, N-(4-aminobutyl)-5-chloro-, hydrochloride (1:1)
w-13

Chemical & Physical Properties

[ Boiling Point ]:
523.4ºC at 760 mmHg

[ Melting Point ]:
241-243ºC

[ Molecular Formula ]:
C14H18Cl2N2O2S

[ Molecular Weight ]:
349.276

[ Flash Point ]:
270.3ºC

[ Exact Mass ]:
348.046600

[ PSA ]:
80.57000

[ LogP ]:
5.48440

[ Storage condition ]:
2-8°C

[ Water Solubility ]:
H2O: Stock solutions of 5 mM are recommended. These stocks should be stable for up to 6 months when stored at 4?#x00b0;C.soluble

MSDS

Safety Information

[ Safety Phrases ]:
22-24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2935009090

Customs

[ HS Code ]: 2935009090

[ Summary ]:
2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%

Articles

Calmodulin antagonists induce cell cycle arrest and apoptosis in vitro and inhibit tumor growth in vivo in human multiple myeloma.

BMC Cancer 14 , 882, (2014)

Human multiple myeloma (MM) is an incurable hematological malignancy for which novel therapeutic agents are needed. Calmodulin (CaM) antagonists have been reported to induce apoptosis and inhibit tumo...

The calmodulin inhibitor CGS 9343B inhibits voltage-dependent K(+) channels in rabbit coronary arterial smooth muscle cells.

Toxicol. Appl. Pharmacol. 285 , 207-13, (2015)

We investigated the effects of the calmodulin inhibitor CGS 9343B on voltage-dependent K(+) (Kv) channels using whole-cell patch clamp technique in freshly isolated rabbit coronary arterial smooth mus...

Quiescence and γH2AX in neuroblastoma are regulated by ouabain/Na,K-ATPase.

Br. J. Cancer 106 , 1807-15, (2012)

Cellular quiescence is a state of reversible proliferation arrest that is induced by anti-mitogenic signals. The endogenous cardiac glycoside ouabain is a specific ligand of the ubiquitous sodium pump...


More Articles


Related Compounds

  • N-[3-methyl-1-(propan-2-yl)-1H-pyrazol-5-yl]-1,3-benzothiazole-2-carboxamide
  • (E)-N-(1-isopropyl-3-methyl-1H-pyrazol-5-yl)-3-(thiophen-2-yl)acrylamide
  • (E)-3-(2-chlorophenyl)-N-(1-isopropyl-3-methyl-1H-pyrazol-5-yl)acrylamide
  • 2-methanesulfonyl-N-[3-methyl-1-(propan-2-yl)-1H-pyrazol-5-yl]benzamide
  • N-(1-isopropyl-3-methyl-1H-pyrazol-5-yl)-2-(methylthio)benzamide
  • N-[3-methyl-1-(propan-2-yl)-1H-pyrazol-5-yl]-2-(4-methylphenyl)acetamide
  • 2,5-dimethoxy-N-[3-methyl-1-(propan-2-yl)-1H-pyrazol-5-yl]benzamide
  • N-[3-methyl-1-(propan-2-yl)-1H-pyrazol-5-yl]-2-(naphthalen-2-yl)acetamide
  • N-Benzyl-5-(3-methyl-1H-indazol-5-yl)oxazol-2-amine
  • n-(4-Methoxybenzyl)-5-(pyridin-4-yl)oxazol-2-amine
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.