(4-Bromophenyl)acetaldehyde
95%
- Product Code: 47586
CAS:
27200-79-9
Molecular Weight: | 199.05 g./mol | Molecular Formula: | C₈H₇BrO |
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EC Number: | MDL Number: | MFCD02261728 | |
Melting Point: | Boiling Point: | 267.5°C at 760 mmHg | |
Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
(4-Bromophenyl)acetaldehyde is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block for the synthesis of various biologically active compounds, including potential drug candidates. The bromine atom on the phenyl ring enhances its reactivity, making it useful in cross-coupling reactions, such as Suzuki or Heck reactions, which are essential for creating complex molecular structures. Additionally, it is employed in the development of fragrances and flavoring agents due to its aldehyde functional group, which contributes to its aromatic properties. In research, it is utilized to study reaction mechanisms and to develop new synthetic methodologies.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | White to Yellow Solid |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,730.00 |
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1.000 | 10-20 days | ฿4,840.00 |
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5.000 | 10-20 days | ฿17,520.00 |
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(4-Bromophenyl)acetaldehyde
(4-Bromophenyl)acetaldehyde is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block for the synthesis of various biologically active compounds, including potential drug candidates. The bromine atom on the phenyl ring enhances its reactivity, making it useful in cross-coupling reactions, such as Suzuki or Heck reactions, which are essential for creating complex molecular structures. Additionally, it is employed in the development of fragrances and flavoring agents due to its aldehyde functional group, which contributes to its aromatic properties. In research, it is utilized to study reaction mechanisms and to develop new synthetic methodologies.
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