[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde
- Product Name
- [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde
- CAS No.
- 1373338-09-0
- Chemical Name
- [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde
- Synonyms
- 1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyd;[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde;[1,2,4]Triazolo[1,5-a]pyridine-2-carboxaldehyde
- CBNumber
- CB62710215
- Molecular Formula
- C7H5N3O
- Formula Weight
- 147.13
- MOL File
- 1373338-09-0.mol
[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde Property
- Density
- 1.39±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- pka
- 0.08±0.30(Predicted)
- Appearance
- White to off-white Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
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
- A180522
- Product name
- [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde
- Purity
- 95+%
- Packaging
- 100mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- CD11270131
- Product name
- [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde
- Purity
- 95+%
- Packaging
- 100mg
- Price
- $248
- Updated
- 2021/12/16
- Product number
- A180522
- Product name
- [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $311
- Updated
- 2021/12/16
- Product number
- CD11270131
- Product name
- [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $386
- Updated
- 2021/12/16
- Product number
- 61-10773
- Product name
- [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde
- Purity
- 95-98%
- Packaging
- 1g
- Price
- $430
- Updated
- 2021/12/16
[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde Chemical Properties,Usage,Production
Synthesis
265643-91-2
1373338-09-0
[1,2,4]Triazolo[1,5-a]pyridin-2-ylmethanol (0.35 g, 2.3 mmol) was used as the raw material, which was dissolved in ethanol (50 mL), and manganese dioxide (IV) (1.02 g, 11.5 mmol) was added. The reaction mixture was heated to reflux for 2 days. After completion of the reaction, it was cooled to room temperature and the solids were removed by diatomaceous earth filtration. The filtrate was concentrated and the resulting residue was purified by reversed-phase column chromatography (eluent: 10% v/v aqueous acetonitrile containing 0.01% NH3-H2O) to afford [1,2,4]triazolo[1,5-a]pyridine-2-carboxaldehyde (0.15 g, 43% yield) as a white solid.ESI MS: m/z 148 [M + H]+.
References
[1] Patent: US2012/178748, 2012, A1. Location in patent: Page/Page column 39
[2] Patent: WO2012/52451, 2012, A1. Location in patent: Page/Page column 119-120
[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde Preparation Products And Raw materials
Raw materials
Preparation Products
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