1-[(4-Methylphenyl)sulfonyl]-1H-imidazole

1-[(4-Methylphenyl)sulfonyl]-1H-imidazole
  • CAS No.:2232-08-8
Other grades of this product :
1-[(4-Methylphenyl)sulfonyl]-1H-imidazole Basic information
Product Name:1-[(4-Methylphenyl)sulfonyl]-1H-imidazole
Synonyms:1-(P-TOLUENESULFONYL)IMIDAZOLE;1-(P-TOLUENESULFONYL)-1H-IMIDAZOLE;1-TOSYLIMIDAZOLE;1-(TOLUENE-4-SULFONYL)IMIDAZOLE;Tosylimidazole;1-(p-toluenesulphonyl)imidazole;1H-IMIDAZOLE, 1-[(4-METHYLPHENYL)SULFONYL]-;1-(Toluene-4-sulfonyl)-1H-imidazole
CAS:2232-08-8
MF:C10H10N2O2S
MW:222.26
EINECS:218-771-9
Product Categories:Building Blocks;Chemical Synthesis;Biochemistry;Condensation & Active Esterification;Heterocyclic Building Blocks;Imidazoles;Coupling Reagent;Condensing Agents (DNA / RNA Synthesis);Nucleosides, Nucleotides & Related Reagents;Protecting Agents, Phosphorylating Agents & Condensing Agents;Synthetic Organic Chemistry
Mol File:2232-08-8.mol
1-[(4-Methylphenyl)sulfonyl]-1H-imidazole Chemical Properties
Melting point 76-78 °C(lit.)
Boiling point 409.1±38.0 °C(Predicted)
density 1.3038 (rough estimate)
refractive index 1.5650 (estimate)
storage temp. Inert atmosphere,Room Temperature
solubility chloroform: soluble25mg/mL, clear, colorless to faintly yellow
form Crystals or Crystalline Powder
pka1.22±0.10(Predicted)
color White to slightly yellow
Sensitive Moisture Sensitive
BRN 612451
InChIKeyYJYMYJRAQYREBT-UHFFFAOYSA-N
CAS DataBase Reference2232-08-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-24/25
WGK Germany 3
10-21
HS Code 29332900
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
1-[(4-Methylphenyl)sulfonyl]-1H-imidazole Usage And Synthesis
Chemical Propertieswhite to slightly yellow crystals
UsesAlcohols to azides in one step.1
Uses1-(p-Toluenesulfonyl)imidazole was used in the synthesis of cationic water soluble cyclodextrin, mono-6A-(1-butyl-3-imidazolium)-6A-deoxy-β-cyclodextrin chloride (BIMCD), useful in chiral separation of amino acids and anionic pharmaceuticals by capillary electrophoresis.
Synthesis Reference(s)The Journal of Organic Chemistry, 45, p. 547, 1980 DOI: 10.1021/jo01291a044
General Description1-(p-Toluenesulfonyl)imidazole converts alcohols to azides in one step.

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