5-(4-CHLOROPHENYL)-2-FURALDEHYDE
5-(4-CHLOROPHENYL)-2-FURALDEHYDE Basic information
- Product Name:
- 5-(4-CHLOROPHENYL)-2-FURALDEHYDE
- Synonyms:
-
- AURORA KA-4235
- ART-CHEM-BB B004122
- ASISCHEM N16482
- 5-(4-CHLOROPHENYL)FURFURAL
- 5-(4-CHLORO-PHENYL)-FURAN-2-CARBALDEHYDE
- 5-(4-CHLOROPHENYL)-2-FURALDEHYDE
- 5-(4-CHLOROPHENYL)-2-FURANCARBOXALDEHYDE
- AKOS BAR-0548
- CAS:
- 34035-03-5
- MF:
- C11H7ClO2
- MW:
- 206.63
- Product Categories:
-
- API intermediates
- Mol File:
- 34035-03-5.mol
5-(4-CHLOROPHENYL)-2-FURALDEHYDE Chemical Properties
- Melting point:
- 128-131 °C (lit.)
- Boiling point:
- 350.7±32.0 °C(Predicted)
- Density
- 1.282±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- Needles
- color
- Pale brown
- CAS DataBase Reference
- 34035-03-5(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36-37/39
- WGK Germany
- 3
- HazardClass
- IRRITANT
- HS Code
- 29321900
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
5-(4-CHLOROPHENYL)-2-FURALDEHYDE Usage And Synthesis
Chemical Properties
Pale brown needles
Uses
5-(4-Chlorophenyl)furfural is a metabolite of Azimilide (A926950, 2 HCl); an oral type III potassium channel blocker agent that blocks both the rapid activating component and the slow activating component of the delayed rectifier potassium current. Both preclinical and clinical studies have demonstrated the efficacy of Azimilide and its safety in the treatment of supraventricular and ventricular tachyarrhythmia. Azimilide is also being studied in a worldwide multicenter trial for prevention of sudden cardiac death in patients after myocardial infarction.
Uses
5-(4-Chlorophenyl)furfural was used as one of the aldehydes in the synthesis of uridine-based library.
General Description
5-(4-Chlorophenyl)furfural is a furfural derivative.
Synthesis
98-01-1
106-47-8
34035-03-5
The target compounds 5-(4-chlorophenyl)-2-furancarboxaldehyde (1-9) were synthesized using 2-furancarboxaldehyde and 4-chloroaniline as starting materials and the reaction was carried out with reference to the methodology reported in the literature [3,13] and the structures were confirmed by appropriate characterization means.
References
[1] Heterocyclic Communications, 2003, vol. 9, # 6, p. 625 - 628
[2] Synthetic Communications, 2005, vol. 35, # 3, p. 333 - 340
[3] Asian Journal of Chemistry, 2013, vol. 25, # 14, p. 7738 - 7742
[4] Asian Journal of Chemistry, 2017, vol. 29, # 4, p. 735 - 741
[5] Russian Journal of Organic Chemistry, 2009, vol. 45, # 9, p. 1375 - 1381
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5-(4-CHLOROPHENYL)-2-FURALDEHYDE(34035-03-5)Related Product Information
- 5-(2 4-DICHLOROPHENYL)FURFURAL 97
- 5-(4-CHLOROPHENYL)-2-FURALDEHYDE
- 5-(3 4-DICHLOROPHENYL)FURFURAL 97
- 5-(2-CHLOROPHENYL)-2-FURALDEHYDE
- 5-(3-CHLOROPHENYL)-2-FURALDEHYDE
- Furfural
- 5-(4-CHLOROPHENYL)-2-FUROIC ACID
- 2-CHLORO-5-(5-FORMYL-FURAN-2-YL)BENZOIC ACID METHYL ESTER
- 5-(4-CHLORO-2-NITRO-PHENYL)-FURAN-2-CARBOXYLIC ACID
- ASISCHEM W57383
- ETHYL 5-(4-CHLOROPHENYL)-2-FORMYL-3-FUROATE
- 5-(4-CHLORO-3-NITRO-PHENYL)-FURAN-2-CARBALDEHYDE
- ASISCHEM R44416
- 5-(4-BROMO-2-CHLOROPHENYL)-2-FURALDEHYDE
- 5-(3-chlorophenyl)-2-furaldehyde [4-[(2-furylmethyl)amino]-6-(4-methoxyanilino)-1,3,5-triazin-2-yl]hydrazone
- SPECS AK-968/37129155
- 2,2-DIBROMO-1-[5-(2,4-DICHLOROPHENYL)-2-FURYL]-1-ETHANONE
- 2-BROMO-1-[5-(2,4,6-TRICHLOROPHENYL)-2-FURYL]ETHAN-1-ONE