Basic information Safety Supplier Related

5-Chloro-1-methylimidazole

Basic information Safety Supplier Related

5-Chloro-1-methylimidazole Basic information

Product Name:
5-Chloro-1-methylimidazole
Synonyms:
  • TIMTEC-BB SBB004296
  • 1H-Imidazole, 5-chloro-1-methyl-
  • 5-CHLORO-1-METHYLIMIDAZOLE
  • 5-CHLORO-1-METHYL-1H-IMIDAZOLE
  • 1-METHYL-5-CHLOROIMIDAZOLE
  • 2-[(3-methylphenyl)thio]-1H-quinazolin-4-one
  • 5-Chloro-1-methylimidazde
  • 5-Chloro-1-MethylImidazole(ForAzathiopurine)
CAS:
872-49-1
MF:
C4H5ClN2
MW:
116.55
EINECS:
212-827-6
Product Categories:
  • Heterocycles
  • Intermediates
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Imidazoles
  • ImidazolesBuilding Blocks
  • Building Blocks
  • Chemical Synthesis
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Heterocycles series
  • Imidazol&Benzimidazole
  • Imidaxoles
Mol File:
872-49-1.mol
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5-Chloro-1-methylimidazole Chemical Properties

Melting point:
82-85°C(11 mmHg)
Boiling point:
82-85 °C/11 mmHg (lit.)
Density 
1.25 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.511(lit.)
Flash point:
205 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Soluble in chloroform and insoluble in water
pka
5.31±0.10(Predicted)
form 
Oil
color 
Colorless to yellow to brown liquid
Water Solubility 
insoluble
BRN 
110509
InChI
InChI=1S/C4H5ClN2/c1-7-3-6-2-4(7)5/h2-3H,1H3
InChIKey
NYDGOZPYEABERA-UHFFFAOYSA-N
SMILES
C1N(C)C(Cl)=CN=1
CAS DataBase Reference
872-49-1(CAS DataBase Reference)
NIST Chemistry Reference
5-Chloro-1-methylimidazole(872-49-1)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933299090

MSDS

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5-Chloro-1-methylimidazole Usage And Synthesis

Chemical Properties

Pale Yellow Oil

Uses

A useful synthetic intermediate.

Uses

5-Chloro-1-methylimidazole is a labelled useful synthetic intermediate.

General Description

5-Chloro-1-methylimidazole is a 5-halo-1-methylimidazole. It participates in electron-rich iron(III) porphyrin complex catalyzed epoxidation of olefins.

Synthesis

615-35-0

872-49-1

The general procedure for the synthesis of 5-chloro-1-methylimidazole from N,N'-dimethyl oxalamide was as follows: phosphorus pentachloride (383.2 g, 1.8 mol) was added to N,N'-dimethyl oxalamide (116.1 g, 1.0 mol), and heated to 60 °C to form a melt with foam generation. Subsequently, the reaction mixture was stirred at 85-95 °C for 2 h, and then distilled to remove the resulting POCl3. The dark brown residue was dissolved in 700 mL of water and adjusted to pH 8 with 915 g of 12.75% KOH solution. The aqueous phase was extracted four times with 500 mL of dichloromethane (DCM), and the organic extracts were combined and dried over sodium sulfate. After concentration under reduced pressure, the resulting reddish brown liquid was vacuum distilled to give 5-chloro-1-methylimidazole (53.1 g, 46% yield) as a colorless liquid. The product properties were as follows: flash point 85-86 °C (22 mbar); 1H NMR (400 MHz, d6-DMSO) δ 7.33 (s, 1H, 4-H), 6.80 (s, 1H, 2-H), 3.47 (s, 3H, CH3); 13C NMR (100 MHz, d6-DMSO) δ 137.4 (C-2), 126.0 (C -4), 118.4 (C-5), 31.6 (CH3).

References

[1] Indian Journal of Chemistry - Section B Organic Chemistry Including Medicinal Chemistry, 1989, vol. 28, # 5, p. 391 - 396
[2] Patent: US2017/281501, 2017, A1. Location in patent: Paragraph 0272-0276
[3] Journal of Organic Chemistry, 2010, vol. 75, # 4, p. 1047 - 1060
[4] Archiv der Pharmazie, 1988, vol. 321, # 4, p. 193 - 197
[5] Journal of Medicinal Chemistry, 1996, vol. 39, # 14, p. 2690 - 2695

5-Chloro-1-methylimidazole Preparation Products And Raw materials

Raw materials

Preparation Products

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