159448-53-0

Basic information

• Product Name: 1-(2-bromo-phenyl)-pentane-1,4-dione
• Synonyms: 1-(2-bromo-phenyl)-pentane-1,4-dione
• CAS NO: 159448-53-0
• Molecular Weight: 255.111
• Mol File: 159448-53-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-(2-bromo-phenyl)-pentane-1,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-bromo-phenyl)-pentane-1,4-dione(159448-53-0)
• EPA Substance Registry System: 1-(2-bromo-phenyl)-pentane-1,4-dione(159448-53-0)

Safety Data

• Hazardous Substances Data: 159448-53-0(Hazardous Substances Data)

Upstream product

• 7732-18-5 water 
• 78-94-4 methyl vinyl ketone 
• 6630-33-7 ortho-bromobenzaldehyde 
• 67-64-1 acetone 
• 2039-88-5 2-bromostyrene 

Downstream Products

• 164460-39-3 2-butyl-4-chloro-5-(hydroxymethyl)-1-<<2-<2-(methoxycarbonyl)phenyl>furan-5-yl>methyl>-1H-imidazole 
• 164460-40-6 2-[5-(2-Butyl-5-chloro-4-hydroxymethyl-imidazol-1-ylmethyl)-furan-2-yl]-benzoic acid methyl ester 
• 159448-42-7 methyl 2-<2-(bromomethyl)furan-5-yl>benzoate 
• 159448-56-3 methyl 2-(5-methylfuran-2-yl)benzoate 
• 159448-55-2 2-(5-methylfuran-2-yl)benzoic acid 
• 159448-54-1 2-(o-bromophenyl)-5-methylfuran 

Relevant articles and documents

Copper-Catalyzed Decarboxylative Oxyalkylation of Alkynyl Carboxylic Acids: Synthesis of ?-Diketones and ?-Ketonitriles

A novel copper-catalyzed decarboxylative oxyalkylation of alkynyl carboxylic acids with ketones and alkylnitriles via direct C(sp3)-H bond functionalization to construct new C-C bonds and C-O double bonds was developed. This transformation is featured by wide functional group compatibility and the use of readily available reagents, thus affording a general approach to ?-diketones and ?-ketonitriles. A possible mechanism is proposed.

Synthesis of furans, pyrroles and pyridazines by a ruthenium-catalysed isomerisation of alkynediols and in situ cyclisation

Alkyne-1,4-diols are readily available substrates which are isomerised to 1,4-diketones using Ru(PPh3)3(CO)H2/xantphos as a catalyst. In situ cyclisation into furans, pyrroles and pyridazines has been achieved under suitable conditions.

Imidazole ethers having a II antagonist activity

Compounds of general formula (I) STR1 wherein E is O or S; R is C 1 -C 5 straight, branched or cyclic alkyl or C 2 -C 5 alkenyl; X can be H, F, Cl, Br, I, CF 3 ; n is an integer 1 to 4; m is an integer 0 to 4; A and B are 5- or 6- membered aromatic carboc