4-(2H-1,2,3-TRIAZOL-2-YL)BENZALDEHYDE
- Product Name
- 4-(2H-1,2,3-TRIAZOL-2-YL)BENZALDEHYDE
- CAS No.
- 179056-04-3
- Chemical Name
- 4-(2H-1,2,3-TRIAZOL-2-YL)BENZALDEHYDE
- Synonyms
- 4-(2H-1,2,3-Triazol-2-yl);4-(triazol-2-yl)benzaldehyde;4-[1,2,3]Triazol-2-ylbenzaldehyde;4-(2H-1,2,3-TRIAZOL-2-YL)BENZALDEHYDE
- CBNumber
- CB1837234
- Molecular Formula
- C9H7N3O
- Formula Weight
- 173.17
- MOL File
- 179056-04-3.mol
4-(2H-1,2,3-TRIAZOL-2-YL)BENZALDEHYDE Property
- Melting point:
- 100-102 °C
- Boiling point:
- 356.8±44.0 °C(Predicted)
- Density
- 1.25±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- -0.08±0.22(Predicted)
- Appearance
- White to off-white Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- P000143208
- Product name
- 4-(2H-1,2,3-Triazol-2-yl)benzaldehyde
- Purity
- 97%
- Packaging
- 100mg
- Price
- $61
- Updated
- 2021/12/16
- Product number
- P000143208
- Product name
- 4-(2H-1,2,3-Triazol-2-yl)benzaldehyde
- Purity
- 97%
- Packaging
- 250mg
- Price
- $98
- Updated
- 2021/12/16
- Product number
- P000143208
- Product name
- 4-(2H-1,2,3-Triazol-2-yl)benzaldehyde
- Purity
- 97%
- Packaging
- 1g
- Price
- $244
- Updated
- 2021/12/16
- Product number
- 9391AA
- Product name
- 4-(2H-1,2,3-Triazol-2-yl)benzaldehyde
- Packaging
- 1g
- Price
- $412
- Updated
- 2021/12/16
- Product number
- CHM0372604
- Product name
- 4-(2H-1,2,3-TRIAZOL-2-YL)BENZALDEHYDE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $496.57
- Updated
- 2021/12/16
4-(2H-1,2,3-TRIAZOL-2-YL)BENZALDEHYDE Chemical Properties,Usage,Production
Uses
4-(2H-1,2,3-Triazol-2-yl)benzaldehyde is useful in the synthesis of cholesterol O-acyltransferase inhibitors.
Synthesis
288-36-8
459-57-4
41498-10-6
179056-04-3
To a solution of 4-fluorobenzaldehyde (2 g, 16 mmol) in DMF (50 mL) was added 1H-1,2,3-triazole (1.32 g, 19.2 mmol) and potassium carbonate (3.3 g, 24 mmol) under the protection of argon and stirred at room temperature. The reaction mixture was then heated to 100 °C and stirred continuously for 5 hours. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was diluted with ice-cold water (35 mL) and extracted with ethyl acetate (2 x 40 mL). The organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography using 20% ethyl acetate/hexane as eluent to give compound 418 (800 mg, 29% yield); switching to 40% ethyl acetate/hexane elution to give compound 419 (1 g, 36% yield), both as yellow solids.
References
[1] Journal of Medicinal Chemistry, 1998, vol. 41, # 13, p. 2390 - 2410
[2] Patent: WO2015/138895, 2015, A1. Location in patent: Paragraph 000338
4-(2H-1,2,3-TRIAZOL-2-YL)BENZALDEHYDE Preparation Products And Raw materials
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Preparation Products
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