4-Bromobenzaldehyde
₹2,600.00
Applications
4-Bromobenzaldehyde is part of a group of benzaldehydes that have in vivo antibacterial activity against Mycobacterium tuburculosis. 4-Bromobenzaldehyde is also used as a reagent in the synthesis of 4-Bromobenzaldehyde semicarbazone, a trial compound of a novel class of anticonvulsants.
Description
4-Bromobenzaldehyde is a chemical compound that belongs to the group of aromatic compounds. It has been shown to have a potent stimulatory effect on locomotor activity in mice, which may be due to its ability to increase levels of epidermal growth factor and gamma-aminobutyric acid in the brain.
Preparation
First, exchange via metal halogen and use the formylation at 0 DEG C of formyl radical source to prepare 2-fluoro-4-bromobenzaldehyde. After crystallisation, this intermediate and methyl alcohol are reacted in the presence of potassium carbonate. Subsequently, 4-bromo-Benzaldehyde,2-methoxy crystallization is made.
Chemical Properties
white crystalline solid
Definition
4-Bromobenzaldehyde is a chemical compound that belongs to the group of aromatic compounds. It has been shown to have a potent stimulatory effect on locomotor activity in mice, which may be due to its ability to increase levels of epidermal growth factor and gamma-aminobutyric acid in the brain.
Description
| Product Name | 4-Bromobenzaldehyde |
| Purity % | >99% |
| CAS Number | 1122-91-4 |
| Chemical Formula | C7H5BrO |
| Usage/Application | END USE |
| Synonyms | p-Bromobenzaldehyde, Benzaldehyde |
| Appearance | off white to yellowish crystalli |
| Type | Syntheses Material Intermedia |
| MF | C7H5BrO |
| Else impurity | 0.5% max |
| Melting point | 55-58 °C(lit.) |
| Boiling point | 66-68°C 2mm |
| Density | 1.85 g/cm3 |
| refractive index | 1.5727 (estimate) |
| Flash point | 228 °F |
| storage temp | Store below +30°C |
| solubility | Chloroform, Ethyl Acetate |
| form | Crystalline Solid |
| color | White |
| Water Solubility | INSOLUBLE |
| Sensitive | Air Sensitive |
Employed in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes. Also used in a cross-coupling study with potassium vinyltrifluoroborate
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