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T-1123
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T-1123

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T-1123
T-1123.svg
Names
Preferred IUPAC name
N,N-Diethyl-N-methyl-3-[(methylcarbamoyl)oxy]anilinium iodide
Other names
AR-16, TL-1217
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
  • InChI=1S/C13H20N2O2.HI/c1-5-15(4,6-2)11-8-7-9-12(10-11)17-13(16)14-3;/h7-10H,5-6H2,1-4H3;1H
    Key: XYPQGNNSAIEXIS-UHFFFAOYSA-N
  • CC[N+](C)(CC)C1=CC(=CC=C1)OC(=O)NC.[I-]
Properties
C13H21IN2O2
Molar mass 364.227 g·mol−1
Related compounds
Related compounds
Neostigmine
Miotine
Hazards
Lethal dose or concentration (LD, LC):
129 μg/kg (Subcutaneous, mice)
75 μg/kg (Subcutaneous, cats)
75 μg/kg (Subcutaneous, dogs)
150 μg/kg (Subcutaneous, rabbits)
122.5 μg/kg (Intramuscular, rats)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

T-1123 is a carbamate-based acetylcholinesterase inhibitor. It was investigated as a chemical warfare agent starting in 1940. It does not go through the blood-brain barrier due to the charge on quaternary nitrogen. The antidote is atropine. T-1123 is a quaternary ammonium ion. A phenyl carbamate ester is bonded in the meta position to the nitrogen on a diethylmethyl amine. The chloride and methylsulfate salt of T-1123 is TL-1299 and TL-1317, respectively.

Synthesis

T-1123 can be produced from m-diethylaminophenol, methyl isocyanate and methyl iodide. First, m-diethylaminophenol is reacted with methyl isocyanate to produce a methylcarbamate. The resulting methylcarbamate is then reacted with methyl iodide to produce T-1123.

See also

Extra reading


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