missing translation for 'onlineSavingsMsg'
Learn More
Learn More
4-Acetylpyridine, 98%, Thermo Scientific Chemicals
40.20 € - 373.00 €
Chemical Identifiers
| CAS | 1122-54-9 |
|---|---|
| Molecular Formula | C7H7NO |
| Molecular Weight (g/mol) | 121.139 |
| MDL Number | MFCD00006433 |
| InChI Key | WMQUKDQWMMOHSA-UHFFFAOYSA-N |
| Synonym | 4-acetylpyridine, methyl 4-pyridyl ketone, ethanone, 1-4-pyridinyl, ketone, methyl 4-pyridyl, 1-pyridin-4-yl ethan-1-one, 1-pyridin-4-yl ethanone, pyridine, 4-acetyl, 4-acetyl pyridine, 4-pyridyl methyl ketone, unii-g47437iow7 |
| PubChem CID | 14282 |
| IUPAC Name | 1-pyridin-4-ylethanone |
| SMILES | CC(=O)C1=CC=NC=C1 |
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|
11469862
|
Thermo Scientific Alfa Aesar
A12015.14 |
25 g |
40.20 €
25g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
|
11479862
|
Thermo Scientific Alfa Aesar
A12015.22 |
100 g |
107.00 €
100g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
|
11489862
|
Thermo Scientific Alfa Aesar
A12015.36 |
500 g | N/A | ||||||
Description
4-acetylpyridine on reaction with - and 4-formylpyridine (H3FoPyS, H4FoPyS) yields semicarbazones. Reaction of acetylpyridine with thiophene-2-carboxaldehyde afforded the 2-chloro-6-ethoxy-4-β-(2-thienyl)acryloylpyridine, which was reacted with malononitrile in refluxing ethanol in the presence of piperidine as a catalyst to afford the cyanoaminopyrane derivative.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications4-acetylpyridine on reaction with - and 4-formylpyridine (H3FoPyS, H4FoPyS) yields semicarbazones. Reaction of acetylpyridine with thiophene-2-carboxaldehyde afforded the 2-chloro-6-ethoxy-4-β-(2-thienyl)acryloylpyridine, which was reacted with malononitrile in refluxing ethanol in the presence of piperidine as a catalyst to afford the cyanoaminopyrane derivative.
Solubility
Insoluble in water. Soluble in alcohol.
Notes
Store in cool place. Keep away from oxidizing agents.
Chemical Identifiers
| 1122-54-9 | |
| 121.139 | |
| WMQUKDQWMMOHSA-UHFFFAOYSA-N | |
| 14282 | |
| CC(=O)C1=CC=NC=C1 |
| C7H7NO | |
| MFCD00006433 | |
| 4-acetylpyridine, methyl 4-pyridyl ketone, ethanone, 1-4-pyridinyl, ketone, methyl 4-pyridyl, 1-pyridin-4-yl ethan-1-one, 1-pyridin-4-yl ethanone, pyridine, 4-acetyl, 4-acetyl pyridine, 4-pyridyl methyl ketone, unii-g47437iow7 | |
| 1-pyridin-4-ylethanone |
Specifications
| 1122-54-9 | |
| 1.103 | |
| 104°C (219°F) | |
| 1.535 | |
| 107629 | |
| Insoluble in water. Soluble in alcohol. | |
| CC(=O)C1=CC=NC=C1 | |
| 121.139 | |
| 121.14 | |
| 4-Acetylpyridine |
| 14°C to 16°C | |
| 210°C to 212°C | |
| C7H7NO | |
| MFCD00006433 | |
| 4-acetylpyridine, methyl 4-pyridyl ketone, ethanone, 1-4-pyridinyl, ketone, methyl 4-pyridyl, 1-pyridin-4-yl ethan-1-one, 1-pyridin-4-yl ethanone, pyridine, 4-acetyl, 4-acetyl pyridine, 4-pyridyl methyl ketone, unii-g47437iow7 | |
| WMQUKDQWMMOHSA-UHFFFAOYSA-N | |
| 1-pyridin-4-ylethanone | |
| 14282 | |
| 98% |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
missing translation for 'einecsNumber' : 214-350-9
missing translation for 'rtecsNumber' : OB5426000
missing translation for 'tsca' : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only
Spot an opportunity for improvement?Share a Content Correction
Product Content Correction
Your input is important to us. Please complete this form to provide feedback related to the content on this product.
Product Title