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Bromo phenyl acetone taj pharma
 

 Bromo phenyl acetone

Molecular Formula : C9H9BrO
 

Name : 1-Bromo-1-phenyl-2-propanone
Synonyms : 1-Bromo-1-phenylacetone, 1-Bromo-1-phenyl-2-propanone, 1-Bromo-1-phenylacetone,

CAS No.: 23022-83-5
Molecular Formula : C9H9BrO
Molecular Weight : 213.07
Purity : 98%
Density : 1.607
Boiling point :  427 șC
Flash point : 114 șC

Description : colorless or slightly yellow liquid.

Production methods : Quorum benzene; 20L propiophenone joined 100L enamelled 11:50. Pot maintain negative pressure (vacuum about MUSCLE), mixing in the next hour was added dropwise 8L bromine, temperature maintained at 30 ° C, bromination reaction after blowing dry air with the exception of the reaction liquid hydrogen bromide, in bromo phenyl acetone benzene 60-65L. Removal of solvent benzene, derived products.

Purposes : Rodenticide enemy of the rat intermediates

Abstract
The photoinitiation efficiency of the free-radical polymerization of methyl methacrylate and styrene by several carbonly compounds has been determined. The compounds considered were -substituted ketones and -dicarbonyl compounds. For the ketones, the initiation efficiency employing methyl methacrylate depends on the substitution; the values obtained change from less than 10-3 (acetone) to 0.65 (3-hydroxy-3-methyl-2-butanone). All ketones are more efficient towards methyl methacrylate than styrene. This result can be explained in terms of triplet quenching by the last monomer. The results obtained employing -dicarbonyl compounds do not conform to a simple pattern. In particular, benzil shows a considerably larger efficiency towards styrene than for methyl methacrylate. Since benzil is efficiently quenched by styrene, the initiation must involve the interaction of an excited benzil molecule and the monomer.




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