4-(Chloromethyl)-1H-imidazole hydrochloride

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4-(Chloromethyl)-1H-imidazole hydrochloride manufacturers

4-(Chloromethyl)-1H-imidazole hydrochloride Basic information
Product Name:4-(Chloromethyl)-1H-imidazole hydrochloride
Synonyms:5-(CHLOROMETHYL)-1H-IMIDAZOLE HYDROCHLORIDE;4-chloromethyl-imidazolhydrochloride;4-Chloromethy-1(3)H-imidazole Hydrochlorid;4-Chloromethy-1H-imidazole Hydrochloride;1H-Imidazole, 4-(chloromethyl)-, monohydrochloride (9CI);4-(Chloromethyl)-1H-imidazole hydrochloride;1H-IMidazole, 4-(chloroMethyl)-, Monohydrochloride;1H-Imidazole, 5-(chloromethyl)-, hydrochloride (1:1)
CAS:38585-61-4
MF:C4H6Cl2N2
MW:153.01
EINECS:
Product Categories:Heterocycles
Mol File:38585-61-4.mol
4-(Chloromethyl)-1H-imidazole hydrochloride Structure
4-(Chloromethyl)-1H-imidazole hydrochloride Chemical Properties
Melting point 1400C
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Ethanol, Methanol, Tetrahydrofuran, Toluene
form Solid
color Beige
InChI1S/C4H5ClN2.ClH/c5-1-4-2-6-3-7-4;/h2-3H,1H2,(H,6,7);1H
InChIKeyFASMXPUFMXBVRL-UHFFFAOYSA-N
SMILESClCC1=CNC=N1.[H]Cl
Safety Information
Hazard Codes Xi
WGK Germany WGK 3
HS Code 2933299090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Toxicitymouse,LD50,intravenous,180mg/kg (180mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#05103,
MSDS Information
4-(Chloromethyl)-1H-imidazole hydrochloride Usage And Synthesis
Chemical PropertiesBeige Solid
Uses4-Chloromethyl-1H-imidazole Hydrochloride (cas# 38585-61-4) is a compound useful in organic synthesis.
Synthesis
4-Imidazolemethanol hydrochloride

32673-41-9

4-(Chloromethyl)-1H-imidazole hydrochloride

38585-61-4

(A) Synthesis of 4-(chloromethyl)-1H-imidazole hydrochloride (1) 2 mL of thionyl chloride was dissolved in 20 mL of toluene followed by the addition of 700 mg of 4-hydroxymethylimidazole hydrochloride. The reaction mixture was heated to the reflux temperature of toluene and maintained for 3 hours. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated to dryness under reduced pressure. 4-(Chloromethyl)-1H-imidazole hydrochloride was finally obtained as a white solid (790 mg, 99% yield).

References[1] Journal of Organic Chemistry, 1990, vol. 55, # 6, p. 1890 - 1901
[2] Patent: US5218115, 1993, A
[3] Journal of Organic Chemistry, 2008, vol. 73, # 21, p. 8591 - 8593
[4] Patent: US4847383, 1989, A
[5] Annales pharmaceutiques francaises, 1998, vol. 56, # 6, p. 250 - 255
4-(Chloromethyl)-1H-imidazole hydrochloride Preparation Products And Raw materials
Raw materials4-Imidazolemethanol hydrochloride-->Toluene-->Thionyl chloride
Preparation ProductsImidazole-4-methanol
Tag:4-(Chloromethyl)-1H-imidazole hydrochloride(38585-61-4) Related Product Information
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