Bromo phenyl
acetone
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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 ºC
Flash point : 114 ºC |
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.
Note:
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those that are used in the manufacture of the controlled substances and
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Note /Government Notification:
N/A
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