2-bromoacetaldehyde
98%, 10% w/w in DCM
- Product Code: 149654
CAS:
17157-48-1
| Molecular Weight: | 122.95 g./mol | Molecular Formula: | C₂H₃BrO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01733508 | |
| Melting Point: | 136-138 °C (lit.) | Boiling Point: | 93.7 °C at 760 mmHg (lit.) |
| Density: | Storage Condition: | -20°C, avoid light, argon-filled |
Product Description:
Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It plays a key role in the preparation of heterocyclic compounds due to its reactivity as an alkylating agent. Commonly employed in the synthesis of imidazoles, thiazoles, and other nitrogen-containing rings found in bioactive molecules. Also utilized in the manufacture of dyes and functionalized polymers where bromine serves as a leaving group for further substitution reactions. Its aldehyde group allows for condensation reactions, making it valuable in forming carbon-carbon bonds. Handle with care due to high reactivity and potential lachrymatory effects.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | liquid |
| Concentration | 9-11 |
| Solvent | DCM |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | £86.85 |
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| 0.100 | 10-20 days | £479.93 |
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| 0.250 | 10-20 days | £1,096.99 |
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| 1.000 | 10-20 days | £3,882.89 |
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2-bromoacetaldehyde
Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It plays a key role in the preparation of heterocyclic compounds due to its reactivity as an alkylating agent. Commonly employed in the synthesis of imidazoles, thiazoles, and other nitrogen-containing rings found in bioactive molecules. Also utilized in the manufacture of dyes and functionalized polymers where bromine serves as a leaving group for further substitution reactions. Its aldehyde group allows for condensation reactions, making it valuable in forming carbon-carbon bonds. Handle with care due to high reactivity and potential lachrymatory effects.
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