5543-98-6

Basic information

• Product Name: 2-(4-Hydroxyphenyl)-1,2-diphenyl-ethanone
• Synonyms: 2-(4-Hydroxyphenyl)-1,2-diphenyl-ethanone;2-(p-Hydroxyphenyl)-2-phenyl-acetophenone
• CAS NO: 5543-98-6
• Molecular Formula: C₂₀H₁₆O₂
• Molecular Weight: 288.33984
• Product Categories: Aromatics;Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 5543-98-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Solubility: Chloroform, Methanol
• CAS DataBase Reference: 2-(4-Hydroxyphenyl)-1,2-diphenyl-ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-Hydroxyphenyl)-1,2-diphenyl-ethanone(5543-98-6)
• EPA Substance Registry System: 2-(4-Hydroxyphenyl)-1,2-diphenyl-ethanone(5543-98-6)

Safety Data

• Hazardous Substances Data: 5543-98-6(Hazardous Substances Data)

Usage

Chemical Properties

Tan Powder

Uses

Photoinitiator in the curing of hexanediol diacrylate. Intermediate in the preparation of clomiphene and tamoxifen analogs.

Upstream product

• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 108-95-2 phenol 
• 6652-29-5 2-phenoxy-1,2-diphenylethanone 
• 5543-97-5 2-(4-methoxyphenyl)-1,2-diphenylethan-1-one 
• 100-66-3 methoxybenzene 
• 451-40-1 phenyl benzyl ketone 
• 540-38-5 p-Iodophenol 

Downstream Products

• 153777-85-6 2-(4-β-chloroethoxyphenyl)-1,2-diphenyl-ethan-1-one 
• 151835-01-7 2-(4-benzyloxyphenyl)-1,2-diphenyl-ethan-1-one 
• 90421-44-6 2-[4-(2-Oxo-1,2-diphenyl-ethoxy)-phenyl]-1,2-diphenyl-ethanone 
• 101-53-1 p-benzylphenol 
• 65-85-0 benzoic acid 
• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 108-95-2 phenol 
• 69967-79-9 ICI 77949 
• 97818-83-2 chloro-tam 
• 153777-92-5 (R,S)-1-(4-benzyloxyphenyl)-1,2-diphenyl-butan-2-ol 
• 153777-86-7 (trans)-1-chloro-2-(4-β-chloroethoxyphenyl)-1,2-diphenylethene 
• 90421-45-7 2-(2,3-Diphenyl-benzofuran-5-yl)-1,2-diphenyl-ethanone 
• 68684-63-9 1-(4-hydroxyphenyl)-1,2-diphenylbut-1-ene 
• 1443223-61-7 C₂₂H₂₀O 

Relevant articles and documents

PROCESS FOR CREATING CARBON-CARBON BONDS USING CARBONYL COMPOUNDS

The present invention concerns a process for preparing a compound of formula (I) by reaction between a compound of formula (II) and a compound of formula (III) in the presence of a copper-containing catalyst, a ligand and base. The invention also concerns the implementing of this process for the preparation of building blocks to prepare molecules of interest in particular in the pharmaceutical, agro-chemical fields, etc.

Reaction of pyrylium salts with nucleophiles. 23: Triarylethene derivatives containing an oxyalkyleneamino or oxyalkylene-N-pyridinium side chain

A synthetic design was devised for preparing primary amines related to anticancer drugs clomiphene and tamoxifen on the basis of key intermediates with a phenolic group, to which a side chain (ω-aminoethoxy or ω- aminopropoxy) was attached. These compound