Contents

N,N-Dimethyl-2-chloro-2-phenylethylamine

N,N-Dimethyl-2-chloro-2-phenylethylamine

Names
IUPAC name 2-Chloro-N,N-dimethyl-2-phenylethanamine
Identifiers
CAS Number	6407-17-6
3D model (JSmol)	Interactive image
ChemSpider	180619
PubChem CID	208446
UNII	F2WN67C3SK Y
CompTox Dashboard (EPA)	DTXSID101283012
InChI InChI=1S/C10H14ClN/c1-12(2)8-10(11)9-6-4-3-5-7-9/h3-7,10H,8H2,1-2H3 Key: BHDHMUNVUMGSIY-UHFFFAOYSA-N
SMILES CN(C)CC(c1ccccc1)Cl
Properties
Chemical formula	C10H14ClN
Molar mass	183.68 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Chemical compound

N,N-Dimethyl-2-chloro-2-phenylethylamine (DMEA) is chemical compound that irreversibly inhibits the acetylcholinesterase. DMEA can cause intoxication in cats, resulting from respiratory failure to death, and progressive damage to the central nervous system in rats.^[1] Synthesis of DMEA can be obtained by treating N,N-dimethyl-2-hydroxy-2-phenylethylamine with thionyl chloride (SOCl₂).^[2] This compound, when dissolved water, decomposes into a highly reactive aziridinium ion, N,N-dimethyl-2-phenylaziridinium (DPA). DPA binds to the anionic site of acetylcholinesterase, where it alkylates and irreversibly inhibits the enzyme.^[3][2] DMEA was also compared to N, N-dimethyl, 2-chloro-2-phenyl-1-methylethyl-amine (M-DMEA) and the results show that there is a difference between the degree of adrenergic blocking activity and their immonium ring stability in vitro. ^[4]

See also[edit]

• Acetylcholinesterase inhibitor

References[edit]

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