Chlorisondamine diiodide

Suppliers

Names

[ CAS No. ]:
96750-66-2

[ Name ]:
Chlorisondamine diiodide

[Synonym ]:
4,5,6,7-Tetrachlor-2-methyl-2-(2-trimethylammonio-aethyl)-isoindolinium,Dijodid
trimethyl-[2-[4,5,6,7-tetrachloro-2-(tritritiomethyl)-1,3-dihydroisoindol-2-ium-2-yl]ethyl]azanium
4,5,6,7-tetrachloro-2-methyl-2-[2-(trimethylammonium)ethyl]isoindolinium diiodide
chlorisondamine iodide
4,5,6,7-Tetrachloro-2,3-dihydro-2-methyl-2-[2-(trimethylammonio)ethyl]-2H-isoindolium diiodide
4,5,6,7-tetrachloro-2-methyl-2-(2-trimethylammonio-ethyl)-isoindolinium,diiodide

Chemical & Physical Properties

[ Molecular Formula ]:
C14H20Cl4I2N2

[ Molecular Weight ]:
611.94

[ Exact Mass ]:
609.84700

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07, GHS09

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H400

[ Precautionary Statements ]:
P273

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn: Harmful;N: Dangerous for the environment;

[ Risk Phrases ]:
22-50

[ Safety Phrases ]:
60-61

[ RIDADR ]:
UN 3077 9 / PGIII

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Tetrachlorophthalic acid
  • N,N-dimethyl-2-(4,5,6,7-tetrachloro-1,3-dihydroisoindol-2-yl)ethanamine
  • methyl iodide
  • Tetrachlorophthalic anhydride

DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Cardiovascular afferents cause the release of 5-HT in the nucleus tractus solitarii; this release is regulated by the low- (PMAT) not the high-affinity transporter (SERT).

J. Physiol. 593(7) , 1715-29, (2015)

The nucleus tractus solitarii (NTS) integrates inputs from cardiovascular afferents and thus is crucial for cardiovascular homeostasis. These afferents primarily release glutamate, although 5-HT has a...

Effects of nicotine and chlorisondamine on cerebral glucose utilization in immobilized and freely-moving rats.

Br. J. Pharmacol. 129 , 147-155, (2000)

Chlorisondamine blocks central nicotinic receptors for many weeks via an unknown mechanism. Intracerebroventricular administration of [(3)H]-chlorisondamine in rats results in an anatomically restrict...

Modulation of neuronal nicotinic acetylcholine receptors by halothane in rat cortical neurons.

Mol. Pharmacol. 59 , 732-743, (2001)

Inhalational general anesthetics have recently been shown to inhibit neuronal nicotinic acetylcholine (ACh) receptors (nnAChRs) expressed in Xenopus laevis oocytes and in molluscan neurons. However, d...


More Articles

Related Compounds

  • CHLORISONDAMINE DIIODIDE
  • Chlorisondamine diiodide
  • dibenzyltellurium diiodide
  • zinc,diiodide,dihydrate
  • dicesium,diiodide
  • dilithium,diiodide
  • 7-fluoro-1,1-dimethyl-2,3-dihydro-1H-inden-5-amine
  • 2-Methyl-6-[(piperazin-1-yl)methyl]quinoline
  • [1-(2-fluoro-6-methylphenyl)-1H-1,2,3-triazol-4-yl]methanol
  • Ethyl 1-chlorocyclopropane-1-carboxylate
  • 2-Methyl-6-[(pyrrolidin-3-yl)methyl]quinoline
  • 5-(2-Methylquinolin-6-yl)-1,3-oxazolidin-2-one
  • N-[2-(2-Oxo-1,3-oxazolidin-3-yl)ethyl]methanesulfonamide
  • 1-Fluorosulfonyloxy-4-isocyanatobenzene
  • 4-cyclopentyl-N,N-dimethylpiperazine-1-sulfonamide
  • (4-Bromo-3-methylphenyl)-(4-methyl-1,4-diazepan-1-yl)methanone
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.