2-(4-Chlorophenyl)thiazole-5-carbaldehyde
2-(4-Chlorophenyl)thiazole-5-carbaldehyde Basic information
- Product Name:
- 2-(4-Chlorophenyl)thiazole-5-carbaldehyde
- Synonyms:
-
- 2-(4-CHLOROPHENYL)THIAZOLE-5-CARBALDEHYDE
- 2-(4-hydroxyphenyl)thiazole-5-carbaldehyde
- 2-(4-chlorophenyl)-1,3-thiazole-5-carbaldehyde
- 5-Thiazolecarboxaldehyde, 2-(4-chlorophenyl)-
- CAS:
- 721920-84-9
- MF:
- C10H6ClNOS
- MW:
- 223.68
- EINECS:
- 200-258-5
- Product Categories:
-
- API intermediates
- Mol File:
- 721920-84-9.mol
2-(4-Chlorophenyl)thiazole-5-carbaldehyde Chemical Properties
- Boiling point:
- 377.6±48.0 °C(Predicted)
- Density
- 1.388±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 0.14±0.10(Predicted)
2-(4-Chlorophenyl)thiazole-5-carbaldehyde Usage And Synthesis
Synthesis
36437-19-1
2521-24-6
721920-84-9
Step 1. Synthesis of 2-(4-chlorophenyl)-1,3-thiazole-5-carbaldehyde. 4-Chlorobenzamide (5 g, 29.1 mmol), magnesium bicarbonate pentahydrate (7.06 g, 14.55 mmol) and 2-chloromalonaldehyde (4.65 g, 43.65 mmol) were added to a flask and the reaction was stirred for 3 hr at 60 °C under nitrogen protection. Upon completion of the reaction, the reaction mixture was allowed to pass through a silica plug for rapid column chromatography and washed with ethyl acetate. The solvent was removed by concentration under reduced pressure to afford the target product 2-(4-chlorophenyl)-1,3-thiazole-5-carbaldehyde (6 g, 92% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 10.06 (s, 1H), 8.43 (s, 1H), 7.99-7.96 (m, 2H), 7.49-7.46 (m, 2H).
References
[1] Patent: WO2004/58761, 2004, A1. Location in patent: Page 37-38
[2] Patent: WO2011/12862, 2011, A1. Location in patent: Page/Page column 102; 109
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2-(4-Chlorophenyl)thiazole-5-carbaldehyde(721920-84-9)Related Product Information
- Fosthiazate
- Chlorodimethylphenylsilane
- Methylchloroisothiazolinone/methylisothiazolinone mixture (MCIT/MIT)
- Benzothiazole
- Triphenylmethyl Chloride
- ETHYL 2-(4-CHLOROPHENYL)-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE
- 1-[2-(4-CHLOROPHENYL)-1,3-THIAZOL-5-YL]-3-(DIMETHYLAMINO)-2-PROPEN-1-ONE
- 2-(4-CHLOROPHENYL)-4-METHYL-1,3-THIAZOLE-5-CARBOXYLIC ACID
- ETHYL 2-(4-CHLOROPHENYL)-4-HYDROXY-1,3-THIAZOLE-5-CARBOXYLATE
- METHYL 2-(4-CHLOROPHENYL)-4-METHYL-1,3-THIAZOLE-5-CARBOXYLATE
- ETHYL 2-(2,4-DICHLOROPHENYL)-4-HYDROXYTHIAZOLE-5-CARBOXYLATE
- 2-(4-Chlorophenyl)thiazole-5-carbaldehyde
- [2-(4-CHLOROPHENYL)-1,3-THIAZOL-5-YL](PHENYL)METHANONE
- [1,1'-BIPHENYL]-4-YL[2-(4-CHLOROPHENYL)-1,3-THIAZOL-5-YL]METHANONE
- 3-[2-(4-CHLOROPHENYL)-1,3-THIAZOL-5-YL]-3-OXOPROPANAL O-(2-[3-(TRIFLUOROMETHYL)PHENOXY]ETHYL)OXIME
- (4-BROMOPHENYL)[2-(4-CHLOROPHENYL)-1,3-THIAZOL-5-YL]METHANONE
- [2-(4-CHLOROPHENYL)-1,3-THIAZOL-5-YL](3,4-DICHLOROPHENYL)METHANONE
- 2-(4-CHLOROPHENYL)-4-METHYL-N-[3-(TRIFLUOROMETHYL)PHENYL]-1,3-THIAZOLE-5-CARBOXAMIDE