2-Pyridinecarbonitrile,6-(1-methylethyl)-(9CI)
- CAS No.
- 337904-76-4
- Chemical Name:
- 2-Pyridinecarbonitrile,6-(1-methylethyl)-(9CI)
- Synonyms
- 6-Isopropylpicolinonitrile;2-Cyano-6-isopropylpyridine;6-Isopropylpyridine-2-carbonitrile;6-(propan-2-yl)pyridine-2-carbonitrile;6-(1-methylethyl)-2-Pyridinecarbonitrile;2-Pyridinecarbonitrile, 6-(1-methylethyl)-;2-Pyridinecarbonitrile,6-(1-methylethyl)-(9CI)
- CBNumber:
- CB01302253
- Molecular Formula:
- C9H10N2
- Molecular Weight:
- 146.19
- MDL Number:
- MFCD18384527
- MOL File:
- 337904-76-4.mol
- MSDS File:
- SDS
SAFETY
Risk and Safety Statements
| Symbol(GHS) | ![]() GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H302-H315-H319-H335 |
| Precautionary statements | P261-P280-P301+P312-P302+P352-P305+P351+P338 |
| HS Code | 2933399990 |
2-Pyridinecarbonitrile,6-(1-methylethyl)-(9CI) price
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Biosynth | MNA90476 | 2-Cyano-6-isopropylpyridine | 337904-76-4 | 100mg | $347 | 2026-06-04 | Buy |
| Biosynth | MNA90476 | 2-Cyano-6-isopropylpyridine | 337904-76-4 | 1g | $885 | 2026-06-04 | Buy |
| Apolloscientific | OR923642 | 2-Cyano-6-isopropylpyridine 95% | 337904-76-4 | 250mg | $307 | 2026-06-04 | Buy |
| Apolloscientific | OR923642 | 2-Cyano-6-isopropylpyridine 95% | 337904-76-4 | 1g | $755 | 2026-06-04 | Buy |
| Activate Scientific | AS12639 | 2-Cyano-6-isopropylpyridine 95% | 337904-76-4 | 250mg | $200 | 2026-06-04 | Buy |
2-Pyridinecarbonitrile,6-(1-methylethyl)-(9CI) Chemical Properties, Uses, Production
Synthesis
65257-53-6
7677-24-9
337904-76-4
1B: General procedure for the synthesis of 2-cyano-6-isopropylpyridine (105). A mixture of 2-isopropylpyridine-N-oxide (104, 1.33 g, 9.7 mmol) with trimethylcyanosilane (TMS-CN, 1.42 mL, 1.06 g, 11.0 mmol) in 1,2-dichloroethane (40 mL) was stirred at room temperature for 5 min. Subsequently, diethylcarbamoyl chloride (Et2NCOCl, 1.23 mL, 9.7 mmol) was added and stirring was continued at room temperature under inert atmosphere. After 2 days of reaction, 10% aqueous potassium carbonate solution was added and stirring was continued for 10 min. The organic layer was separated and the aqueous layer was extracted twice with 1,2-dichloroethane. The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate, 3:1) to afford 6-isopropylpyridinecarbonitrile 1.06 g (74% yield): m/z = 147 (M + H)+.
References
[1] Patent: WO2007/14926, 2007, A1. Location in patent: Page/Page column 108
[2] European Journal of Inorganic Chemistry, 2006, # 2, p. 366 - 379
[3] Bioorganic and Medicinal Chemistry Letters, 1998, vol. 8, # 5, p. 453 - 458
2-Pyridinecarbonitrile,6-(1-methylethyl)-(9CI) Preparation Products And Raw materials
Raw materials
Preparation Products
2-Pyridinecarbonitrile,6-(1-methylethyl)-(9CI) Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
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