1-Methyl-1H-1,2,3-triazole-5-carbaldehyde
- CAS No.
- 202931-88-2
- Chemical Name:
- 1-Methyl-1H-1,2,3-triazole-5-carbaldehyde
- Synonyms
- 3-methyltriazole-4-carbaldehyde;1-Methyl-1H-1,2,3-triazole-5-carbaldehyde;3-Methyl-3H-[1,2,3]triazole-4-carbaldehyde;1H-1,2,3-Triazole-5-carboxaldehyde, 1-methyl-
- CBNumber:
- CB52595875
- Molecular Formula:
- C4H5N3O
- Molecular Weight:
- 111.1
- MDL Number:
- MFCD10696346
- MOL File:
- 202931-88-2.mol
- MSDS File:
- SDS
SAFETY
Risk and Safety Statements
| Symbol(GHS) | ![]() GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H302-H335-H315-H319 |
| Precautionary statements | P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P |
1-Methyl-1H-1,2,3-triazole-5-carbaldehyde price More Price(26)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Activate Scientific | AS114604 | 1-Methyl-1H-1,2,3-triazole-5-carbaldehyde 95% | 202931-88-2 | 100mg | $267 | 2026-06-04 | Buy |
| Activate Scientific | AS114604 | 1-Methyl-1H-1,2,3-triazole-5-carbaldehyde 95% | 202931-88-2 | 250mg | $294 | 2026-06-04 | Buy |
| Activate Scientific | AS114604 | 1-Methyl-1H-1,2,3-triazole-5-carbaldehyde 95% | 202931-88-2 | 1g | $686 | 2026-06-04 | Buy |
| Matrix Scientific | 133373 | 1-Methyl-1H-1,2,3-triazole-5-carbaldehyde | 202931-88-2 | 250.00mg | $1620 | 2026-05-18 | Buy |
| Synthonix | M40133 | 1-Methyl-1H-1,2,3-triazole-5-carbaldehyde 95+% | 202931-88-2 | 100mg | $120 | 2026-05-06 | Buy |
1-Methyl-1H-1,2,3-triazole-5-carbaldehyde Chemical Properties, Uses, Production
Synthesis
16681-65-5
68-12-2
202931-88-2
1.6 M n-butyllithium (0.9 mL, 1.4 mmol) was added slowly and dropwise to a tetrahydrofuran (THF, 10 mL) solution of 1-methyl-1H-1,2,3-triazole (32.0 mg, 1.2 mmol) at -78 °C, ensuring that the reaction temperature was maintained below -60 °C. After the reaction mixture was stirred continuously at -78 °C for 30 min, N,N-dimethylformamide (0.14 mL, 1.8 mmol) was added. Subsequently, the reaction system was slowly warmed to room temperature and stirring was continued for 1 hour. Upon completion of the reaction, the reaction was quenched with water and extracted with ethyl acetate (3 × 10 mL). The organic phases were combined, washed with water (3 x 10 mL), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography with an eluent ratio of 95:5 to 100:0 dichloromethane to methanol, resulting in 1-methyl-1H-1,2,3-triazole-5-carboxaldehyde as a yellow oil (40 mg, 30% yield).1H NMR (CDCl3) data: δ 4.10 (s, 3H), 7.88 (s, 1H), 9.55 (s, 1H). 1H).
References
[1] ACS Medicinal Chemistry Letters, 2015, vol. 6, # 6, p. 650 - 654
[2] Patent: WO2008/135826, 2008, A2. Location in patent: Page/Page column 157; 158
[3] Patent: US2014/107094, 2014, A1. Location in patent: Paragraph 0625; 0626
[4] Patent: US2015/105372, 2015, A1. Location in patent: Paragraph 0304; 0305
[5] Patent: WO2015/57206, 2015, A1. Location in patent: Page/Page column 74; 75
1-Methyl-1H-1,2,3-triazole-5-carbaldehyde Preparation Products And Raw materials
Raw materials
Preparation Products
1-Methyl-1H-1,2,3-triazole-5-carbaldehyde Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
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