345-66-4

Basic information

• Product Name: Methanone, (4-fluoro-3-methylphenyl)phenyl-
• CAS NO: 345-66-4
• Molecular Formula: C14H11FO
• Molecular Weight: 214.239
• Mol File: 345-66-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Methanone, (4-fluoro-3-methylphenyl)phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (4-fluoro-3-methylphenyl)phenyl-(345-66-4)
• EPA Substance Registry System: Methanone, (4-fluoro-3-methylphenyl)phenyl-(345-66-4)

Safety Data

• Hazardous Substances Data: 345-66-4(Hazardous Substances Data)

Upstream product

• 95-52-3 2-Fluorotoluene 
• 98-88-4 benzoyl chloride 
• 51437-00-4 5-bromo-2-fluorotoluene 
• 345-65-3 C₁₄H₁₃FO 
• 100-52-7 benzaldehyde 
• 452-75-5 4-chloro-2-fluorotoluene 
• 403-15-6 4-fluoro-3-methyl-benzoic acid 
• 455-84-5 4-fluoro-3-methylbonzoyl chloride 
• 71-43-2 benzene 

Downstream Products

• 85588-41-6 6-fluoro-3-benzoylphenyl acetonitrile 
• 834895-47-5 3-(3-methoxy-4-pyrrolidinophenyl)-3-phenyl-3H-naphtho[2,1-b]pyran 
• 834895-46-4 3-(3-methyl-4-pyrrolidinophenyl)-3-phenyl-3H-naphtho[2,1-b]pyran 
• 834895-60-2 1-(3-methyl-4-pyrrolidinophenyl)-1-phenylprop-2-yn-1-ol 
• 834895-54-4 3-methyl-4-pyrrolidinobenzophenone 
• 85588-38-1 3-bromomethyl-4-fluoro benzophenone 

Relevant articles and documents

Intramolecular Charge Transfer Controls Switching Between Room Temperature Phosphorescence and Thermally Activated Delayed Fluorescence

Chemical modification of phenothiazine-benzophenone derivatives tunes the emission behavior from triplet states by selecting the geometry of the intramolecular charge transfer (ICT) state. A fundamental principle of planar ICT (PICT) and twisted ICT (TICT

Synthesis and photochromic properties of substituted 3H-naphtho[2,1-b] pyrans

The synthesis and spectroscopic properties of novel 3H-naphtho[2,1-b]pyrans are described. Subtle variation of the colour of the photo-generated merocyanine dyes derived from these naphthopyrans can be accomplished by controlling the steric interactions between a terminal pyrrolidine donor group and a proximal substituent.

6-Halogen derivatives of 2-(3-benzoylphenyl)propionic acid.

The synthesis of the 6-fluoro (I a), 6-chloro (I b) and 6-bromo (I c) derivatives of the known antiinflammatory agent 2-(3-benzoylphenyl)propionic acid (ketoprofen) is reported. The procedure employed involves the direct phase-transfer methylation of the