4-[(Dimethylamino)methyl]benzonitrile
![4-[(Dimethylamino)methyl]benzonitrile Structure](CAS/GIF/35525-86-1.gif)
- CAS No.
- 35525-86-1
- Chemical Name:
- 4-[(Dimethylamino)methyl]benzonitrile
- Synonyms
- 4-cyano-N,N-dimethylbenzylamine;Benzonitrile,4-[(diMethylaMino)Methyl]-
- CBNumber:
- CB01490437
- Molecular Formula:
- C10H12N2
- Molecular Weight:
- 160.22
- MDL Number:
- MFCD00029578
- MOL File:
- 35525-86-1.mol
- MSDS File:
- SDS
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H302-H315-H319-H332-H335 |
| Precautionary statements | P261-P280-P305+P351+P338 |
| HS Code | 2926907090 |
4-[(Dimethylamino)methyl]benzonitrile price More Price(30)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | S683116 | 4-(DIMETHYLAMINOMETHYL)BENZONITRILE AldrichCPR | 35525-86-1 | 1 unit | $121 | 2026-04-30 | Buy |
| Sigma-Aldrich | S683116 | 4-(DIMETHYLAMINOMETHYL)BENZONITRILE AldrichCPR | 35525-86-1 | 250mg | $110 | 2024-03-01 | Buy |
| Biosynth | KBA52586 | 4-((Dimethylamino)methyl)benzonitrile | 35525-86-1 | 10g | $354 | 2026-06-04 | Buy |
| Apolloscientific | OR323176 | 4-((Dimethylamino)methyl)benzonitrile 97% | 35525-86-1 | 250mg | $21 | 2026-06-04 | Buy |
| Activate Scientific | AS43475 | 4-((Dimethylamino)methyl)benzonitrile 97% | 35525-86-1 | 1g | $49 | 2026-06-04 | Buy |
4-[(Dimethylamino)methyl]benzonitrile Chemical Properties, Uses, Production
Synthesis
124-40-3
17201-43-3
![4-[(DIMETHYLAMINO)METHYL]BENZONITRILE](/CAS/GIF/35525-86-1.gif)
35525-86-1
GENERAL STEPS: 4-Cyanobenzyl bromide (10 g, 0.05 mol), sodium carbonate (5.95 g, 56.0 mmol, 1.1 eq.) and dimethylamine (56.0 mmol, 1.1 eq.) were dissolved in N,N-dimethylformamide (75 mL) and stirred at room temperature for 3 hours. The reaction mixture was then heated to 90°C to continue the reaction. After completion of the reaction, it was cooled to room temperature, water (200 mL) was added and stirred at 0°C. The reaction was carried out at 0°C with the addition of water. If crystals precipitated, they were collected by filtration, washed with cold water (2 x 50 mL) and dried under vacuum to give the first products. The filtrates were combined and extracted with ethyl acetate (3 x 50 mL), the organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the second product. The total yield of the products was 72-98%.
References
[1] Angewandte Chemie - International Edition, 2007, vol. 46, # 46, p. 8869 - 8871
[2] Collection of Czechoslovak Chemical Communications, 1987, vol. 52, # 8, p. 2095 - 2106
[3] European Journal of Medicinal Chemistry, 2018, vol. 152, p. 31 - 52
[4] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 17, p. 5891 - 5908
[5] Archiv der Pharmazie, 1962, vol. 295 /67, p. 690 - 697
4-[(Dimethylamino)methyl]benzonitrile Preparation Products And Raw materials
Raw materials
Preparation Products
4-[(Dimethylamino)methyl]benzonitrile Suppliers
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