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27996-86-7

27996-86-7 Structure

27996-86-7 Structure
IdentificationMore
[Name]

4-(1H-1,2,4-TRIAZOL-1-YL)BENZALDEHYDE
[CAS]

27996-86-7
[Synonyms]

4-[1,2,4]TRIAZOL-1-YL-BENZALDEHYDE
4-(1H-1,2,4-TRIAZOL-1-YL)BENZALDEHYDE
4-(1H-1,2,4-TRIAZOL-1-YL)BENZENECARBALDEHYDE
BUTTPARK 95\50-81
4-(1h-1,2,4-triazol-1-yl)benzaldehyde, 95+%
4-[1,2,4]TRIAZOL-1-YL-BENZALDEHYDE, 95+%
[Molecular Formula]

C9H7N3O
[MDL Number]

MFCD02681969
[Molecular Weight]

173.17
[MOL File]

27996-86-7.mol
Chemical PropertiesBack Directory
[Melting point ]

147 °C
[Boiling point ]

369.2±44.0 °C(Predicted)
[density ]

1.25±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

slightly sol. in Methanol
[form ]

powder to crystal
[pka]

1.94±0.10(Predicted)
[color ]

Light orange to Yellow to Green
[InChI]

InChI=1S/C9H7N3O/c13-5-8-1-3-9(4-2-8)12-7-10-6-11-12/h1-7H
[InChIKey]

TVEJNWMWDIXPAX-UHFFFAOYSA-N
[SMILES]

C(=O)C1=CC=C(N2C=NC=N2)C=C1
[CAS DataBase Reference]

27996-86-7(CAS DataBase Reference)
Questions And AnswerBack Directory
[Uses]

4-(1-1,2,4-triazolyl)benzaldehyde is a useful research chemical used in organic synthesis and other chemical processes.
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

22-36/37/38
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2913000090
Spectrum DetailBack Directory
[Spectrum Detail]

4-(1H-1,2,4-TRIAZOL-1-YL)BENZALDEHYDE(27996-86-7)1HNMR
4-(1H-1,2,4-TRIAZOL-1-YL)BENZALDEHYDE(27996-86-7)FT-IR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

4-(1H-1,2,4-triazol-1-yl)benzaldehyde(27996-86-7)
Hazard InformationBack Directory
[Synthesis]

1,2,4-Triazole

288-88-0

4-Fluorobenzaldehyde

459-57-4

4-(1H-1,2,4-TRIAZOL-1-YL)BENZALDEHYDE

27996-86-7

GENERAL METHOD: A mixture of 4-fluorobenzaldehyde (10 mmol) and 1,2,4-triazole (10 mmol) was dissolved in anhydrous N,N-dimethylformamide (DMF, 20 mL). Potassium carbonate (K2CO3, 12 mmol) was added to the above stirred solution in portions over 15 minutes. The reaction mixture was stirred at 110°C for 10-12 hours. After completion of the reaction, the heating was stopped and the potassium carbonate was removed by filtration. The filtrate was extracted with ethyl acetate (3 x 15 mL). The organic layers were combined, washed with water (3 x 15 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography (60-120 mesh) with the eluent of methanol:chloroform (1:99, v/v) to obtain the target compound 4-(1-1,2,4-triazolyl)benzaldehyde.

[References]

[1] European Journal of Medicinal Chemistry, 2009, vol. 44, # 7, p. 2930 - 2935
[2] European Journal of Medicinal Chemistry, 2011, vol. 46, # 9, p. 4302 - 4310
[3] Patent: US2012/329649, 2012, A1. Location in patent: Page/Page column 72
[4] Patent: US2014/171314, 2014, A1. Location in patent: Page/Page column
[5] Patent: WO2014/100163, 2014, A1. Location in patent: Page/Page column 131
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