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CAS RN: 7462-74-0 | Product Number: B3380
2-Bromoisobutyramide
Purity: >98.0%(GC)(N)
Synonyms:
- 2-Bromo-2-methylpropionamide
Documents:
Size | Unit Price | Saitama (Kawaguchi) | Hyogo (Amagasaki) | Stock in other WH |
More Stock Info
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5G |
¥6,800
|
Ship in 2-3 business days after ordering |
5 | ||
25G |
¥23,000
|
13 |
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*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
* For the case that without specific estimated shipping data, e.g.: If displayed as "will be shipped after 8 working days", the products will be shipped 8 working days later after ordering.
* Available Stock: Prompt shipment (for products) in Saitama/Hyogo warehouse. Stock in other WH: 2-3 Business Days
* Please contact us if you need further information.
* To send your quote request for bulk quantities, please click on the "Request Bulk Quote" button. Please note that we cannot offer bulk quantities for some products.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.
Specifications
Appearance | White to Almost white powder to crystal |
Purity(GC) | min. 98.0 % |
Purity(with Total Nitrogen) | min. 98.0 % |
Melting point | 145.0 to 149.0 °C |
Properties (reference)
Melting Point | 147 °C |
GHS
Related Laws:
Transport Information:
Application
Aminating Agent Introducing an Amino Group via Smiles Rearrangement
Experimental procedure: To a solution of 487 mg (3 mmol) of 6-hydroxy-3,4-dihydro-1(2H)-naphthalenone in DMA (4.5 mL) is added 360 mg (9 mmol) of sodium hydroxide. The mixture is stirred at room temperature for 1 hour, 1.494 g (9 mmol) of 2-bromoisobutyramide is added and the mixture is stirred at room temperature for 5 hours. After the reaction period, 1.080 g (27 mmol) of sodium hydroxide is added and the resulting mixture is stirred at 50 °C for 1 hour. After the reaction period, 4.5 mL of water is added and the mixture is heated at reflux for 1 hour. Water (9 mL) is added to the solution and cooled slowly to room temperature. The precipitated crystalline powder are collected and washed with 4.5 mL of water three times to give 287 mg (59%) of 6-amino-3,4-dihydro-1(2H)-naphthalenone as off-white crystalline powder.
References
- A New Practical One-Pot Conversion of Phenols to Anilines
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