889-26-9

Basic information

• Product Name: 4-phenoxypropiophenone
• Synonyms: 4-phenoxypropiophenone;1-(4-phenoxyphenyl)proapan-1-one
• CAS NO: 889-26-9
• Molecular Formula: C₁₅H₁₄O₂
• Molecular Weight: 0
• Mol File: 889-26-9.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-phenoxypropiophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenoxypropiophenone(889-26-9)
• EPA Substance Registry System: 4-phenoxypropiophenone(889-26-9)

Safety Data

• Hazardous Substances Data: 889-26-9(Hazardous Substances Data)

Upstream product

• 101-84-8 diphenylether 
• 79-03-8 propionyl chloride 
• 123-62-6 propionic acid anhydride 
• 456-03-1 1-(4-fluorophenyl)propan-1-one 
• 108-95-2 phenol 
• 70-70-2 4-hydroxypropiophenone 
• 5724-03-8 1-(4-fluorophenyl)allyl alcohol 
• 701-47-3 1-(4-fluorophenyl)propanol 
• 459-57-4 4-fluorobenzaldehyde 

Downstream Products

• 60319-66-6 1-phenoxy-4-(prop-1-en-1-yl)benzene 
• 92434-62-3 2-bromo-4'-phenoxyfuropiophenone 
• 124746-46-9 2-{1-(4-Phenoxyphenyl)propan-1-ylidene}-5-methyl-1,3,5-dithiazine 
• 473732-65-9 1-(4-phenoxyphenyl)propan-1-amine 

Relevant articles and documents

Synthesis and optical properties of two cationic cyclopentadienyliron complexes of arene containing the triphenylbutene structure

Two novel cationic cyclopentadienyliron complexes of arene containing the triphenylbutene group (TPBE-Fc) were synthesized and characterized by IR, UV-visible, 1H NMR, and 13C NMR spectroscopy, and by MS. The optical properties of th

Exploring Tandem Ruthenium-Catalyzed Hydrogen Transfer and SNAr Chemistry

A hydrogen-transfer strategy for the catalytic functionalization of benzylic alcohols via electronic arene activation, accessing a diverse range of bespoke diaryl ethers and aryl amines in excellent isolated yields (38 examples, 70% average yield), is reported. Taking advantage of the hydrogen-transfer approach, the oxidation level of the functionalized products can be selected by judicious choice of simple and inexpensive additives.

5-Aryl-imidazolin-2-ones as a scaffold for potent antioxidant and memory-improving activity

A series of 5-phenyl-substituted-N-alkyl-imidazolin-2-ones with potent radical-scavenging activity and lipid peroxidation inhibitory activity was synthesized. Many of the compounds showed memory-improving effect in animal models independent of the inhibitory activity on lipid peroxidation.