Ethyl 3-ethoxy-3-iminopropanoate hydrochloride

CAS: 2318-25-4

Ref. 3D-FE142387

Product Information

• Name: Ethyl 3-ethoxy-3-iminopropanoate hydrochloride
• Synonyms: 1,3-Diethoxy-3-Oxopropan-1-Iminium Chloride, 2-(Ethoxycarbonyl)acetimidic acid ethyl ester hydrochloride, 3-Ethoxy-3-iminopropanoic acid ethyl ester hydrochloride, 3-Ethoxy-3-iminopropionic acid ethyl ester hydrochloride, 3-Ethoxy-3-oxo-1-ethoxypropan-1-imine hydrochloride, Acetic acid, (1-ethoxyformimidoyl)-, ethyl ester, hydrochloride, Ethyl (ethoxycarbonyl)acetimidate hydrochloride, Ethyl 2-(ethoxycarbonyl)acetimidate hydrochloride, Ethyl beta-ethoxy-beta-iminopropionate hydrochloride, Ethyl carbethoxyacetimidate hydrochloride, Ethyl β-ethoxy-β-iminopropionate hydrochloride, Ethyl β-ethoxyl-β-imido-propionate hydrochloride, Ethylβ-ethoxyl-β-imido-propionate hydrochloride, Nsc 104122, Propanoic acid, 3-ethoxy-3-imino-, ethyl ester, hydrochloride, Propanoic acid, 3-ethoxy-3-imino-, ethyl ester, hydrochloride (1:1), β-Ethoxy-β-iminopropionic acid ethyl ester hydrochloride

Description

Ethyl 3-ethoxy-3-iminopropanoate hydrochloride is a synthesized drug that has inhibitory properties on the nervous system. It binds to and blocks the imidazoline receptor, which inhibits the synthesis of the neurotransmitter noradrenaline. This leads to an increase in the amount of acetylcholine, which is a neurotransmitter that stimulates muscle contraction. The imidazoline receptor is insensitive to changes in temperature and pH, and it is not affected by benzodiazepine. Ethyl 3-ethoxy-3-iminopropanoate hydrochloride has been synthetized from nitrophenyl, yielding imidazoline, imidazopyridine, and other products. Nitrophenyl reacts with ethoxyacetylene in a nucleophilic substitution reaction to yield nitrobenzene and ethyl 3-ethoxy-3-iminopropanoate. The nitro group on

• Brand: Biosynth

Chemical properties

• Molecular weight: 195.64 g/mol
• Formula: C₇H₁₃NO₃·ClH
• Purity: Min. 95%