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4-(1H-Imidazol-1-yl)benzaldehyde

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CAS:10040-98-9
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4-(1H-Imidazol-1-yl)benzaldehyde Basic information
Product Name:4-(1H-Imidazol-1-yl)benzaldehyde
Synonyms:4-(5H-Imidazol-1-yl)-benzaldehyde;4-imidazolylbenzaldehyde;4-(1H-IMIDAZOL-1-YL)BENZALDEHYDE 97%;4-(1H-Imidazol-1-yl)benzaldehyde ,97%;4-(1H-lmidazol-1-yl)benzenecarbaldehyde;4-IMIDAZOL-1-YL-BENZA;4-(1H-IMidazol-1-yl)benzaldehyde, GC 97%;BUTTPARK 43\57-13
CAS:10040-98-9
MF:C10H8N2O
MW:172.18
EINECS:
Product Categories:Aldehydes;Building Blocks;C10-C12;Chemical Synthesis;Heterocyclic Building Blocks;Organic Building Blocks;Imidazol&Benzimidazole;Building Blocks;Heterocyclic Building Blocks;Imidazoles;Carbonyl Compounds;Heterocycles
Mol File:10040-98-9.mol
4-(1H-Imidazol-1-yl)benzaldehyde Structure
4-(1H-Imidazol-1-yl)benzaldehyde Chemical Properties
Melting point 153-155 °C(lit.)
Boiling point 351.1±25.0 °C(Predicted)
density 1.15±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility soluble in Methanol
form powder to crystal
pka5.07±0.10(Predicted)
color Light yellow to Yellow to Orange
InChIInChI=1S/C10H8N2O/c13-7-9-1-3-10(4-2-9)12-6-5-11-8-12/h1-8H
InChIKeyDCICUQFMCRPKHZ-UHFFFAOYSA-N
SMILESC(=O)C1=CC=C(N2C=NC=C2)C=C1
CAS DataBase Reference10040-98-9(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HazardClass IRRITANT
HS Code 29332900
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
4-(1H-Imidazol-1-yl)benzaldehyde Usage And Synthesis
Chemical PropertiesWhite to light brown solid
Uses 4-(1H-Imidazol-1-yl)benzaldehyde could be used to synthesis (E)-3-[4-(1H-imidazol-1-yl)phenyl]-1-(4-methylphenyl)prop-2-en-1-one with 4′-methylacetophenone through Claisen–Schmidt condensation. This novel compound is suitable for anti-aspergillus activity study[1].
Synthesis
Imidazole

288-32-4

4-Fluorobenzaldehyde

459-57-4

4-(1H-Imidazol-1-yl)benzaldehyde

10040-98-9

General procedure for the synthesis of 4-(imidazol-1-yl)benzaldehyde from imidazole and p-fluorobenzaldehyde: A mixture of p-fluorobenzaldehyde (25.0 g, 0.200 mol), imidazole (0.300 mol), and anhydrous potassium carbonate (40.0 g) was dissolved in DMF (300 mL) under dry conditions, and catalytic amount of Aliquat 336 reagent was added. The reaction mixture was refluxed at 100 °C for 24 hours. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure and cooled to room temperature. Subsequently, the concentrate was poured into ice water and allowed to stand overnight. The precipitated solid product was filtered, washed with water and recrystallized with methanol to afford the target compound 4-(1H-imidazol-1-yl)benzaldehyde (Ia) in 92% yield as yellow crystals with a melting point of 152°C (in agreement with literature reports) [34,44].

References[1] N. Bailey, Bradley O. Ashburn. “(E)-3-[4-(1H-Imidazol-1-yl)phenyl]-1-(4-methylphenyl)prop-2-en-1-one.” Molbank 1 1 (2021).
4-(1H-Imidazol-1-yl)benzaldehyde Preparation Products And Raw materials
Raw materialsEthyl acetate-->N,N-Dimethylformamide-->Potassium carbonate-->Imidazole-->4-Fluorobenzaldehyde-->4-Bromobenzaldehyde-->4-Iodobenzaldehyde-->Methyl trioctyl ammonium chloride
Tag:4-(1H-Imidazol-1-yl)benzaldehyde(10040-98-9) Related Product Information
1H-Imidazole-4-carbaldehyde 4-Hydroxybenzaldehyde Benzaldehyde p-Anisaldehyde Imidazole 4-Dimethylaminobenzaldehyde 4-(1H-imidazol-1-yl)pyridine sodium benzaldehyde-o-sulfonate 4-(1H-IMIDAZOL-1-YL)BENZOIC ACID 4'-(IMIDAZOL-1-YL)ACETOPHENONE 2-IMIDAZOL-1-YL-BENZALDEHYDE, 95+%,2-IMIDAZOL-1-YL-BENZALDEHYDE 3-METHOXY-4-(4-METHYL-1H-IMIDAZOL-1-YL)BENZALDEHYDE,3-METHOXY-4-(4-METHYL-IMIDAZOL-1-YL)-BENZALDEHYDE Formaldehyde 1-[4-(4,5-DICHLORO-1H-IMIDAZOL-1-YL)PHENYL]ETHAN-1-ONE GLG-V 13 METHYL 4-(1H-IMIDAZOL-1-YL)BENZENECARBOXYLATE BIS[4-(1H-IMIDAZOL-1-YL)PHENYL]METHANONE 3-DIMETHYLAMINO-1-(4-IMIDAZOL-1-YL-PHENYL)-PROPENONE