28122-15-8

Basic information

• Product Name: 2-Buten-1-one, 1-(4-fluorophenyl)-
• Synonyms: 2-Buten-1-one,1-(4-fluorophenyl)
• CAS NO: 28122-15-8
• Molecular Formula: C10H9FO
• Molecular Weight: 164.179
• Mol File: 28122-15-8.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 238.6±32.0 °C(Predicted)
• Density: 1.081±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 2-Buten-1-one, 1-(4-fluorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Buten-1-one, 1-(4-fluorophenyl)-(28122-15-8)
• EPA Substance Registry System: 2-Buten-1-one, 1-(4-fluorophenyl)-(28122-15-8)

Safety Data

• Hazardous Substances Data: 28122-15-8(Hazardous Substances Data)

Upstream product

• 906353-48-8 1-(4-fluorophenyl)-3-hydroxybutan-1-one 
• 403-42-9 1-(4-fluorophenyl)ethanone 
• 63072-14-0 1-(4-fluorophenyl)-2-(triphenyl-λ⁵phosphanylidene)ethanone 
• 75-07-0 acetaldehyde 
• 403-29-2 2-bromo-4'-fluoroacetophenone 
• 582-83-2 1-(4-fluorophenyl)butan-1-one 
• 86718-78-7 1-(4-fluorophenyl)-3-buten-1-ol 
• 61668-02-8 1-(4-fluorophenyl)but-3-en-1-one 
• 459-57-4 4-fluorobenzaldehyde 
• 2251-76-5 2-(4-fluorophenyl)-2-oxoacetic acid 
• 107-18-6 allyl alcohol 
• 15022-08-9 diallylcarbonate 
• 462-06-6 fluorobenzene 
• 625-35-4 trans-chrotonyl chloride 

Downstream Products

• 1114065-80-3 3-((S)-1-(4-bromophenyl)ethylamino)-1-(4-fluorophenyl)butan-1-one 
• 1613249-89-0 C₁₄H₁₅FO₂ 
• 945983-03-9 C₁₇H₁₅Cl₂FO₂S 
• 906353-49-9 3-[3-(4-fluorophenyl)-1-methyl-3-oxopropyl]-1-methylpiperidin-4-one 

Relevant articles and documents

Organocatalytic Enantioselective Selenosulfonylation of a C-C Double Bond to Form Two Stereogenic Centers in an Aqueous Medium

Organocatalytic selenosulfonylation of the C-C double bond of α,β-unsaturated ketones to construct two contiguous stereogenic centers in an aqueous medium was described. A series of α-selenyl and β-sulfonyl ketones with various functional groups were synthesized in good yields and enantioselectivities with saturated NaCl solution as the solvent. In addition, this protocol had been successfully scaled up to a decagram scale via a simple workup procedure.

Environment-friendly method for synthesizing propenyl ketone compound

The invention discloses an environment-friendly method for synthesizing a propenyl ketone compound. The method comprises the following steps: subjecting an aldehyde compound and allyl bromide to a Barbier reaction in the presence of metal powder, so as to obtain an allyl alcohol compound; and subjecting the allyl alcohol compound to a structural isomerization reaction in the presence of a catalyst, thereby obtaining the propenyl ketone compound. The method disclosed by the invention has the advantages of short synthesis route, mild reaction conditions, simplicity in operation, readily available raw materials, and the like and has relatively high academic research value and market economy significance.

Decarboxylative allylation of arylglyoxylic acids with allyl alcohol

A decarboxylative allylation of arylglyoxylic acids with allyl alcohol has been developed. In the presence of catalytic amounts of Pd(dba) 2 and PPh3, the substrates are in an esterification equilibrium with the allyl arylglyoxylates, which are continuously decarboxylated to give α,β-unsaturated ketones along with CO2 and water as the only byproducts.