[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
- Molecular Weight:
- 147.13
- MDL Number:
- MFCD24678370
- MOL File:
- 1373338-09-0.mol
- MSDS File:
- SDS
| Product description | Number | Pack Size | Price |
| [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde 95% | AA009WGF | 100mg | $145 |
| [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde 95% | AA009WGF | 250mg | $232 |
| [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde 95% | AA009WGF | 500mg | $380 |
| [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde 95% | AA009WGF | 1g | $578 |
| [1,2,4]triazolo[1,5-a]pyridine-2-carbaldehyde 97% | P48564 | 250MG | $320 |
SAFETY
Risk and Safety Statements
| Symbol(GHS) | ![]() GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H302-H315-H319-H335 |
| Precautionary statements | P261-P305+P351+P338 |
[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde price More Price(27)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| aablocks | AA009WGF | [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde 95% | 1373338-09-0 | 100mg | $145 | 2026-05-28 | Buy |
| aablocks | AA009WGF | [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde 95% | 1373338-09-0 | 250mg | $232 | 2026-05-28 | Buy |
| aablocks | AA009WGF | [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde 95% | 1373338-09-0 | 500mg | $380 | 2026-05-28 | Buy |
| aablocks | AA009WGF | [1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde 95% | 1373338-09-0 | 1g | $578 | 2026-05-28 | Buy |
| ACHEMBLOCK | P48564 | [1,2,4]triazolo[1,5-a]pyridine-2-carbaldehyde 97% | 1373338-09-0 | 250MG | $320 | 2026-05-27 | Buy |
[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde Chemical Properties,Uses,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
[1,2,4]Triazolo[1,5-a]pyridine-2-carbaldehyde Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
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