30186-16-4

Basic information

• Product Name: Ethanone, 1,1'-(4-hydroxy-1,3-phenylene)bis-
• CAS NO: 30186-16-4
• Molecular Formula: C10H10O3
• Molecular Weight: 178.188
• Mol File: 30186-16-4.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Ethanone, 1,1'-(4-hydroxy-1,3-phenylene)bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1,1'-(4-hydroxy-1,3-phenylene)bis-(30186-16-4)
• EPA Substance Registry System: Ethanone, 1,1'-(4-hydroxy-1,3-phenylene)bis-(30186-16-4)

Safety Data

• Hazardous Substances Data: 30186-16-4(Hazardous Substances Data)

Upstream product

• 7191-41-5 1-(2-hydroxy-5-iodophenyl)ethan-1-one 
• 1350803-03-0 5-ethynyl-2-hydroxyacetophenone 
• 64-19-7 acetic acid 
• 108-95-2 phenol 
• 60-35-5 acetamide 
• 99-93-4 4-Hydroxyacetophenone 
• 7446-70-0 aluminium trichloride 
• 13031-43-1 4-acetyloxyacetophenone 
• 7250-94-4 o-acetoxyacetophenone 
• 75-36-5 acetyl chloride 
• 10192-62-8 2,2-bis(4-acetoxyphenyl)propane 
• 103867-83-0 2-(4-acetoxyphenyl)-2-methyl-1,3-dioxolane 
• 118-93-4 o-hydroxyacetophenone 
• 579-74-8 2-Methoxyacetophenone 

Downstream Products

• 154185-27-0 C₂₈H₂₆O₇ 
• 106924-27-0 ethyl 2,4-bis<1-acetyl-4,5-dihydro-5-(3-methoxyphenyl)pyrazol-3-yl>phenoxyacetate 
• 106924-28-1 ethyl 2,4-bis<1-acetyl-4,5-dihydro-5-(4-methoxyphenyl)pyrazol-3-yl>phenoxyacetate 

Relevant articles and documents

Kinetics and mechanism of certain acetylation reactions with acetamide/oxychloride in acetonitrile under Vilsmeier-Haack conditions

Vilsmeier-Haack (VH) acetylation reactions with benzaldehydes or acetophenones in MeCN followed second-order kinetics and afforded acetyl derivatives under kinetic conditions, irrespective of the nature of the oxychloride (SOCl2 or POCl3/

Acetamide/SO2Cl2 as an efficient reagent for Friedel-Craft's acylation of aromatic compounds under ultrasonic and microwave conditions

Acetamide/SO2Cl2 reagent has been developed for effective Friedel-Craft's acylation of aromatic compounds. Acylation of aromatic compounds with acetamide/SO2Cl2 was much more effective and faster than analogous (acetamide/SOCl2) and (acetamide/POCl 3) reagents even under conventional conditions. However, microwave and ultrasonic assisted reactions afforded high yields of products in very short reaction times (30-40 min under sonication and 3-4 min under microwave assisted conditions).

Synthesis of 2,3-disubstituted-6-chromones of potential medicinal interest

The title compounds (12-19) have been synthesized by the condensation of 2,3-disubstituted-6-chromones (8-11) with hydrazine hydrate in the presence of formic or acetic acid.Their structures have been elucidated on the basis o