Published TCIMAIL newest issue No.201
Maximum quantity allowed is 999
CAS RN: 111562-32-4 | Product Number: P1902
2-(1H-Pyrazol-5-yl)aniline
Purity: >97.0%(GC)
- 5-(2-Aminophenyl)pyrazole
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| Product Number | P1902 |
Purity / Analysis Method
|
>97.0%(GC) |
| Molecular Formula / Molecular Weight | C__9H__9N__3 = 159.19 |
| Physical State (20 deg.C) | Solid |
Storage Temperature
|
Room Temperature (Recommended in a cool and dark place, <15°C) |
| CAS RN | 111562-32-4 |
| Reaxys Registry Number | 5320 |
| PubChem Substance ID | 125307613 |
| MDL Number | MFCD09028476 |
| Appearance | Light yellow to Brown powder to crystal |
| Purity(GC) | min. 97.0 % |
| Purity(Nonaqueous Titration) | min. 95.0 % |
| NMR | confirm to structure |
| Melting Point | 129 °C |
| Pictogram |
|
| Signal Word | Warning |
| Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
| Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
| HS Number | 2933199090 |

A mixture of phenylboronic acid (1) (0.25 mmol) and 2-(1H-pyrazol-5-yl)aniline (0.25 mmol) in toluene (1 mL) is heated under reflux with a Dean-Stark condenser for 1 h. After being cooled to room temperature, the solvent is evaporated in vacuo. To the residue, RuH2(CO)(PPh3)3 (0.0075 mmol) is added. After filling dry nitrogen in the glass tube, norbornene (1.25 mmol), triethylsilane (1.25 mmol) and toluene (0.13 mL) are added under a nitrogen atmosphere. The mixture is heated at 135 °C for 12 h. 2 is isolated by bulb-to-bulb distillation (280-290 °C / 4.7 mmHg, mp 138 °C, Y. 89%) as a white solid.
References
- Easily Attachable and Detachable ortho-Directing Agent for Arylboronic Acids in Ruthenium-Catalyzed Aromatic C−H Silylation
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