412034-14-1

Basic information

• Product Name: 1,4-dimesitylbutane-1,4-dione
• Synonyms: 1,4-dimesitylbutane-1,4-dione
• CAS NO: 412034-14-1
• Molecular Weight: 322.447
• Mol File: 412034-14-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,4-dimesitylbutane-1,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-dimesitylbutane-1,4-dione(412034-14-1)
• EPA Substance Registry System: 1,4-dimesitylbutane-1,4-dione(412034-14-1)

Safety Data

• Hazardous Substances Data: 412034-14-1(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 544-01-4 isopentyl ether 
• 78830-31-6 (E)-1,2-dimesitoylethene 
• 7647-01-0 hydrogenchloride 
• 64-19-7 acetic acid 
• 64-17-5 ethanol 
• 10035-10-6 hydrogen bromide 
• 135-19-3 β-naphthol 
• 60-29-7 diethyl ether 
• 4225-92-7 2-bromo-1-(2,4,6-trimethylphenyl)ethanone 
• 71-43-2 benzene 
• 56-23-5 tetrachloromethane 
• 7732-18-5 water 
• 67-56-1 methanol 

Downstream Products

• 78830-31-6 (E)-1,2-dimesitoylethene 
• 110-15-6 succinic acid 
• 1044-14-0 2,5-Dimesityl-furan 
• 108-67-8 1,3,5-trimethyl-benzene 
• 110330-69-3 3,4-dibromo-2,5-dimesityl-furan 
• 860000-01-7 2,5-Dimesityl-3-nitro-furan 
• 855243-22-0 1,4-dimesityl-butane-1,4-diol 

Relevant articles and documents

One-Pot Synthesis of O-Heterocycles or Aryl Ketones Using an InCl3/Et3SiH System by Switching the Solvent

An efficient one-pot synthesis of O-heterocycles or aryl ketones has been achieved using Et3SiH in the presence of InCl3 via a sequential ionic hydrogenation reaction by switching the solvent. This methodology can be used to construct C-O bonds and to prepare conjugate reduction products, including chromans, tetrahydrofurans, tetrahydropyrans, dihydroisobenzofurans, dihydrochalcones, and 1,4-diones in a facile manner. In addition, a novel plausible mechanism involving a conjugate reduction and a tandem reductive cyclization was verified by experimental investigations.