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4-Methoxybenzamidine, hydrochloride

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4-Methoxybenzamidine, hydrochloride Basic information
Product Name:4-Methoxybenzamidine, hydrochloride
Synonyms:4-ANISAMIDINE HYDROCHLORIDE;4-MethoxybenzamidineHCl;4-MethoxybenzenecarboxiMidaMide Hydrochloride;4-Methoxy-benzenecarboxiMidaMide Hydrochloride;4-Methoxyphenylformamidine hydrochloride;p-Anisamidine hydrochloride;p-Methoxybenzamidine hydrochloride;4-MethoxybenziMidaMide hydrochloride
CAS:51721-68-7
MF:C8H11ClN2O
MW:186.64
EINECS:
Product Categories:Amines;Aromatics Compounds;Aromatics
Mol File:51721-68-7.mol
4-Methoxybenzamidine, hydrochloride Structure
4-Methoxybenzamidine, hydrochloride Chemical Properties
Melting point 218-220°C
storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly), Water (Slightly)
form Solid
color White to Off-White
λmax261nm(H2O)(lit.)
Safety Information
Hazard Codes Xn
Risk Statements 22
HazardClass IRRITANT
HS Code 2916310090
MSDS Information
4-Methoxybenzamidine, hydrochloride Usage And Synthesis
Chemical PropertiesOff-White Crystalline Solid
Uses4-Methoxybenzamidine Hydrochloride (cas# 51721-68-7) is a compound useful in organic synthesis.
Synthesis
Anisonitrile

874-90-8

4-METHOXYBENZAMIDINE, HYDROCHLORIDE

51721-68-7

General procedure for the synthesis of 4-methoxybenzenecarbamidine hydrochloride from 4-methoxybenzyl cyanide: 4-methoxybenzyl cyanide (2.1 g, 15.7 mmol) was mixed with sodium methanolate (86 mg, 1.57 mmol) in 20 mL of anhydrous methanol, and the reaction was stirred for 48 hours at room temperature. Subsequently, ammonium chloride (0.84 g, 15.7 mmol) was added to the reaction system and stirring was continued for 24 hours. After completion of the reaction, the precipitate was collected by filtration, washed with ether and dried under vacuum to afford the target product 4-methoxybenzenecarboximidamide hydrochloride (1.3 g, 44.5% yield). Mass spectrum (ESI) m/z: 151.1 ([M+H]+).

References[1] European Journal of Medicinal Chemistry, 2018, vol. 150, p. 783 - 795
[2] Journal of the American Chemical Society, 1985, vol. 107, # 9, p. 2743 - 2748
[3] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 3, p. 613 - 623
[4] Collection of Czechoslovak Chemical Communications, 1981, vol. 46, # 4, p. 933 - 940
[5] Patent: US6218538, 2001, B1
4-Methoxybenzamidine, hydrochloride Preparation Products And Raw materials
Raw materialsMethanol-->Sodium-->Ammonium chloride-->Anisonitrile-->Ethyl 4-methoxybenzimidate hydrochloride-->Sodium Methoxide
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