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1 See also  





2 References  














EA-3966








 

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From Wikipedia, the free encyclopedia
 


EA-3966
Names
Preferred IUPAC name

N1-({3-[(Dimethylcarbamoyl)oxy]pyridin-2-yl}methyl)-N1,N1,N10,N10,N10-pentamethyldecane-1,10-bis(aminium) dibromide

Identifiers

CAS Number

3D model (JSmol)

CompTox Dashboard (EPA)

  • InChI=1S/C24H46N4O2.2BrH/c1-26(2)24(29)30-23-17-16-18-25-22(23)21-28(6,7)20-15-13-11-9-8-10-12-14-19-27(3,4)5;;/h16-18H,8-15,19-21H2,1-7H3;2*1H/q+2;;/p-2

    Key: SMYJBWHIVMYSPG-UHFFFAOYSA-L

  • [Br-].[Br-].CN(C)C(=O)Oc1cccnc1C[N+](C)(C)CCCCCCCCCC[N+](C)(C)C

Properties

Chemical formula

C24H46Br2N4O2
Molar mass 582.466 g·mol−1
Appearance Crystalline solid
Melting point 139–143 °C (282–289 °F; 412–416 K)

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

EA-3966 is a carbamate nerve agent.[1] It is synthesized by reacting 2-dimethylaminomethyl-3-dimethylcarbamoxypyridine with 10-bromodecyltrimethylammonium bromide.[2]

See also[edit]

References[edit]

  1. ^ Handbook of chemical and biological warfare agents (2nd ed.). CRC Press. 24 August 2007. ISBN 9780849314346.
  • ^ "Chemical agents".
  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=EA-3966&oldid=1223122851"

    Categories: 
    Carbamate nerve agents
    Pyridines
    Quaternary ammonium compounds
    Acetylcholinesterase inhibitors
    Bromides
    Bisquaternary anticholinesterases
    Aromatic carbamates
    Ester stubs
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    This page was last edited on 10 May 2024, at 01:22 (UTC).

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