4-Bromobenzaldehyde diethyl acetal
97%
- Product Code: 119387
Alias:
4-Bromobenzaldehyde diethyl acetal
1-Bromo-4-(diethoxymethyl)benzene
4-Bromobenzaldehyde ethylene acetal
CAS:
34421-94-8
| Molecular Weight: | 259.14 g./mol | Molecular Formula: | C₁₁H₁₅BrO₂ |
|---|---|---|---|
| EC Number: | 000-000-0 | MDL Number: | MFCD01863514 |
| Melting Point: | Boiling Point: | 75 °C0.2 mm Hg(lit.) | |
| Density: | 1.274 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure allows for the introduction of bromine and aldehyde functionalities into complex molecules, making it valuable in the development of active ingredients. Additionally, it is employed in the synthesis of fine chemicals and specialty materials, where its reactivity and stability under specific conditions are advantageous. The compound is also utilized in research settings for the study of chemical reactions involving acetal protection and deprotection strategies.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 97-100 |
| Refractive Index N20/D | 1.511-1.515 |
| Appearance | Colorless Liquid |
| Infrared Spectrum | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,120.00 |
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4-Bromobenzaldehyde diethyl acetal
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure allows for the introduction of bromine and aldehyde functionalities into complex molecules, making it valuable in the development of active ingredients. Additionally, it is employed in the synthesis of fine chemicals and specialty materials, where its reactivity and stability under specific conditions are advantageous. The compound is also utilized in research settings for the study of chemical reactions involving acetal protection and deprotection strategies.
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