cas:1451-82-7 2-Bromo-4-Methylpropiophenone
Whats Is 2-Bromo-4-Methylpropiophenone cas:1451-82-7
2-Bromo-4-Methylpropiophenone, also known as 2-Bromo-1-(4-methylphenyl)propan-1-one, is an organic compound with the chemical formula C10H11BrO and CAS number 1451-82-7. It is a colorless to pale yellow liquid with a distinctive odor. This compound is usually used as an intermediate and raw material in the fine chemistry industry.
2-Bromo-4-Methylpropiophenone cas:1451-82-7 Product Parameter
Product Name: | 2 Bromo 4 Methylpropiophenone |
CAS NO: | 1451-82-7 |
Molecular Weight: | 227.1 |
Molecular Formula: | C10H11BrO |
Boiling Point: | 273ºC |
Melting point: | 75-77ºC |
Density: | 1.357 |
Appearance: | White Powder |
Solubility: | Soluble in chloroform and methanol. |
How To Store 2 bromo 4 methylpropiophenone
2-Bromo-1-(4-methylphenyl)propan-1-one, is an organic compound with the chemical formula C10H11BrO and CAS number 1451-82-7. It is a colorless to pale yellow liquid with a distinctive odor . This compound should be stored in a cool, dry, and well-ventilated area, away from sources of heat and flame. The storage temperature should not exceed 4°C
2 bromo 4 methylpropiophenone Cas 1451-82-7
It is usually used as the intermediate and raw material in the fine chemistry industry. Specifically. Moreover, this compound may function as an effective ingredient to prepare the therapeutically useful 1-phenyl-2-piperidinoalkanol derivatives. In addition, this substance has been demonstrated to be involved in the preparation of a pharmaceutical composition comprising a pyrrole derivative, which shows a desirable activity for the treatment pollakiuria or urinary incontinence.
2-Bromo-4-Methylpropiophenone Uses
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2-Bromo-4-Methylpropiophenone Synthesis
14.8 g (0.1 mol) of 4′-methylpropiophenone are introduced into 100 ml of chloroform, in the presence of a small amount of finely ground aluminium chloride, and a solution of 15.9 g (0.1 mol; 5 ml) of bromine, in 20 ml of chloroform is added dropwise whilst cooling with an ice bath. The mixture is left to react overnight at ambient temperature. It is then filtered, the solvent is evaporated off from the filtrate and the crystalline residue is washed with diethyl ether. 21.5 g of crystals are collected.
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