91860-00-3

Basic information

• Product Name: 3-(1H-imidazol-1-yl)-1,3-diphenylprop-2-en-1-one
• Synonyms: 3-(1H-imidazol-1-yl)-1,3-diphenylprop-2-en-1-one
• CAS NO: 91860-00-3
• Molecular Weight: 274.322
• Mol File: 91860-00-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3-(1H-imidazol-1-yl)-1,3-diphenylprop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1H-imidazol-1-yl)-1,3-diphenylprop-2-en-1-one(91860-00-3)
• EPA Substance Registry System: 3-(1H-imidazol-1-yl)-1,3-diphenylprop-2-en-1-one(91860-00-3)

Safety Data

• Hazardous Substances Data: 91860-00-3(Hazardous Substances Data)

Upstream product

• 288-32-4 1H-imidazole 
• 7338-94-5 1,3-diphenyl-2-propynone 

Downstream Products

• 120-46-7 1,3-diphenylpropanedione 
• 85169-79-5 1-(1,3-diphenyl-3-oxo-1-propen-1-yl)-3-methylimidazolium iodide 
• 144651-59-2 3-pyrrolidino-1,3-diphenyl-2-propen-1-one 
• 1666-86-0 2,4,6-triphenylpyrimidine 
• 22114-29-0 N,N-dimethyl-4,6-diphenylpyrimidin-2-amine 
• 40230-24-8 2-amino-4,6-diphenylpyrimidine 
• 1145-01-3 3,5-Diphenylpyrazole 
• 52790-27-9 3,5-diphenyl-4,5-dihydroisoxazol-5-ol 
• 85143-96-0 1,3-diphenyl-3-(p-methyl)phenoxy-2-propen-1-one 
• 10348-81-9 1,3-Diphenyl-3-phenoxy-propen-⁽²⁾-on-⁽¹⁾ 

Relevant articles and documents

Non-metal catalytic method for preparing 1,3-diketone compounds based on acetyenic ketone

The invention discloses a non-metal catalytic method for preparing 1,3-diketone compounds based on acetyenic ketone. The preparation method is a stepwise method or a one-pot method. The stepwise method comprises the following steps: mixing an acetyenic ketone compound I, a nitrogen-containing aromatic compound II and a No.1 base for a reaction, performing separation and purification to obtain an intermediate product, mixing the intermediate product and a No.2 base for a reaction, and performing separation and purification to obtain the product; and the one-pot method comprises the following steps: firstly mixing an acetyenic ketone compound I and a nitrogen-containing aromatic compound II, adding a No.1 base, performing a reaction for a period of time, adding a No.2 base, continuing a reaction for a period of time, and finally performing separation and purification to obtain the product. The method provided by the invention has mild reaction conditions, simple operation and a higher yield, wherein the yield is generally 80% or more, and the method has greater practical application value in drug synthesis.