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Detail of "5031-78-7"

  • CAS Number:
  • 5031-78-7
  • Name:

  • Ethanone,1-(4-phenoxyphenyl)-

  • Superlist Name:
  • 4'-Phenoxyacetophenone
  • Molecular Structure:
  • Formula:
  • C14H12O2
  • Molecular Weight:
  • 212.24
  • Synonyms:
  • Acetophenone,4'-phenoxy- (6CI,7CI,8CI);1,2-(4-Acetylphenoxy)benzene;1-(4-Phenoxyphenyl)ethanone;4-Acetyldiphenyl ether;4-Acetyldiphenyl oxide;4-Acetylphenyl phenyl ether;NSC 39658;p-Phenoxyacetophenone;
  • Density:
  • 1.108 g/cm3
  • Melting Point:
  • 50-52 °C(lit.)
  • Boiling Point:
  • 345.9 °C at 760 mmHg
  • Flash Point:
  • 148.9 °C
  • Solubility:
  • insoluble in water
  • Appearance:
  • light yellow powder
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/37/38
  • Safety:
  • 26-37/39 Details
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CAS No.5031-78-7 4'-Phenoxyacetophenone

Assay:98%

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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CAS No.5031-78-7 4'-Phenoxyacetophenone

Supplier:Shijiazhuang JuSha Imp. & Exp. Co., Ltd [ China (Mainland)]

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CAS No.5031-78-7 4'-Phenoxyacetophenone

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CAS No.5031-78-7 4'-Phenoxyacetophenone

4'-Phenoxyacetophenone

Supplier:Changzhou Harvest Chemistry Co., Ltd [ China (Mainland)]

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CAS No.5031-78-7 4'-Phenoxyacetophenone

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CAS No.5031-78-7 4'-Phenoxyacetophenone

Molecular Formula：C14H12O2 Purity： 98.0%

Supplier:Taizhou Medicine & Chemical Research Institute [ China (Mainland)]

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CAS No.5031-78-7 4'-Phenoxyacetophenone

4'-Phenoxyacetophenone

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CAS No.5031-78-7 4'-Phenoxyacetophenone

Supplier:Nanjing derhoo chem&tech co.,ltd. [ China (Mainland)]

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Reference

Voltammetric study of phenylaminomethyl derivatives of hydroxyacetophenones
Voltammetric study of phenylaminomethyl derivatives of hydroxyacetophenones. Kuliev, A. M.; Farzaliev, V. M.; Agaeva, E. A.; Mamedova, R. K.; Sardarova, S. H. (Inst. Khim.Some commonly used reagents like 61891-73-4 and 5031-78-7 are used in this experiment. Prisadok, Baku, USSR). Nov. Polyarogr., Tezisy Dokl. Vses. Soveshch. Polyarogr., 6th, 128. Edited by: Stradins, J. "Zinatne": Riga, USSR. (Russian) 1975. CODEN: 34DIA8. DOCUMENT TYPE: Conference CA Section: 72 (Electrochemistry) Section cross-reference(s): 22, 25 The transfer of electrons in these compds. is basically inductive. Electrochem. oxidn. of p-hydroxyacetophenone (I), its phenylaminomethyl derivs., and corresponding derivs. of N-alkylaniline showed that the phenolic substituent plays a minor role in the process. Half-wave potentials of (I) correlated with .sigma.-consts. of the substituents. Direct polar coupling of the substituent with reaction center affected significantly the reaction. .
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