4-(Bromoacetyl)pyridine hydrobromide
90%
- Product Code: 144232
Alias:
2-bromo-1-(4-pyridinyl)-1-acetone hydrobromide; 4-bromoacetylpyridine hydrobromide; 4-(bromoacetyl)pyrimidine hydrobromide; 4-(bromoacetyl)pyridine hydrochloride; 2-bromo-1-(4-pyridinyl) ethyl ketone; 4-(bromoacetyl)pyridine bromate; 4-(bromoethyl)piperidine bromic acid
CAS:
5349-17-7
| Molecular Weight: | 280.94 g./mol | Molecular Formula: | C₇H₇Br₂NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02681893 | |
| Melting Point: | 194 °C | Boiling Point: | 268.3ºC |
| Density: | 1.57g/cm3 | Storage Condition: | 2~8°C |
Product Description:
Used primarily in organic synthesis as an alkylating agent for introducing pyridine moieties into target molecules. It is especially valuable in the preparation of ligands for metal catalysts and in the development of functionalized heterocyclic compounds. Commonly employed in the synthesis of pharmaceutical intermediates due to its ability to selectively modify amines and other nucleophiles. Also utilized in the production of specialty polymers and in biochemical research for labeling or modifying biomolecules. Its reactivity with nucleophiles makes it suitable for constructing complex molecular architectures in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 89.5-100 |
| Appearance | White to yellow powder |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5g | 10-20 days | $68.89 |
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| 25g | 10-20 days | $283.52 |
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| 1g | 10-20 days | $15.90 |
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4-(Bromoacetyl)pyridine hydrobromide
Used primarily in organic synthesis as an alkylating agent for introducing pyridine moieties into target molecules. It is especially valuable in the preparation of ligands for metal catalysts and in the development of functionalized heterocyclic compounds. Commonly employed in the synthesis of pharmaceutical intermediates due to its ability to selectively modify amines and other nucleophiles. Also utilized in the production of specialty polymers and in biochemical research for labeling or modifying biomolecules. Its reactivity with nucleophiles makes it suitable for constructing complex molecular architectures in medicinal chemistry.
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