97060-29-2

Basic information

• Product Name: 2-Buten-1-one, 1-(4-methoxyphenyl)-, (2E)-
• CAS NO: 97060-29-2
• Molecular Formula: C11H12O2
• Molecular Weight: 176.215
• Mol File: 97060-29-2.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: 2-Buten-1-one, 1-(4-methoxyphenyl)-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Buten-1-one, 1-(4-methoxyphenyl)-, (2E)-(97060-29-2)
• EPA Substance Registry System: 2-Buten-1-one, 1-(4-methoxyphenyl)-, (2E)-(97060-29-2)

Safety Data

• Hazardous Substances Data: 97060-29-2(Hazardous Substances Data)

Upstream product

• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 15022-08-9 diallylcarbonate 
• 7099-91-4 p-methoxybenzoylformic acid 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 140846-38-4 1-(4-methoxyphenyl)-2-buten-1-ol 
• 309723-10-2 1-(1-allyloxyallyl)-4-methoxybenzene 
• 84132-74-1 2-(4-methoxyphenyl)-2,5-dihydrofuran 
• 105-13-5 4-Methoxybenzyl alcohol 
• 123-11-5 4-methoxy-benzaldehyde 
• 24165-60-4 1-(4-methoxyphenyl)but-3-en-1-ol 
• 64-17-5 ethanol 
• 768-60-5 4-methoxyphenylacetylen 
• 426840-86-0 1-(1-ethoxybuta-1,3-dienyl)-4-methoxybenzene 
• 4160-51-4 1-(4-methoxyphenyl)-1-butanone 

Downstream Products

• 4160-51-4 1-(4-methoxyphenyl)-1-butanone 
• 97060-65-6 (2'RS,3'RS)- and (2'RS,3'SR)-1-(2',3'-dimethyl-5'-(4-methoxyphenyl)-1',5'-dioxopentyl)pyrrolidine 
• 97060-64-5 (E,2'RS,3'RS)- and (E,2'RS,3'SR)-1-(3'-hydroxy-3'-(4-methoxyphenyl)-2'-methyl-1'-oxo-4'-hexenyl)pyrrolidine 
• 1181379-09-8 4-(4-methoxyphenyl)-2-methyl-4-oxobutanenitrile 
• 1313028-37-3 (S)-4-(4-methoxyphenyl)-2-methyl-4-oxobutanenitrile 
• 1360472-56-5 (R)-4-(4-methoxyphenyl)-2-methyl-4-oxobutanenitrile 
• 1408003-32-6 (Z)-6-acetoxy-4-methyl-6-(4-methoxyphenyl)-5-hexen-2-one 
• 1443249-95-3 1-(4-methoxyphenyl)-3-methyl-4-nitrobutan-1-one 
• 1443249-97-5 (Z)-5-(4-methoxyphenyl)-N-(5-(4-methoxyphenyl)-3-methyl-2H-pyrrol-2-ylidene)-3-methyl-1H-pyrrol-2-amine 
• 1443249-98-6 (Z)-4-(5-(5-(4-methoxyphenyl)-3-methyl-2H-pyrrol-2-ylideneamino)-4-methyl-1H-pyrrol-2-yl)phenol 
• 1443250-02-9 C₂₄H₂₂BF₂N₃O₂ 
• 1443250-08-5 C₂₃H₂₀BF₂N₃O₂ 

Relevant articles and documents

A new and one-pot synthesis of α,β-unsaturated ketones by dehydrogenation of various ketones with n-tert-butyl phenylsulfinimidoyl chloride

α,β-Unsaturated ketones were synthesized by one-pot procedure from various ketones in good to excellent yields on treatment of their lithium enolates with N-tert-butyl phenylsulfinimidoyl chloride (1) under mild conditions.

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.

An iron-catalyzed hydroalkylation reaction of α,β-unsaturated ketones with ethers

A general strategy for the hydroalkylation of vinyl ketones using ethers catalyzed by an iron catalyst is described. This catalytic method permits direct transformation of easily accessible and abundant precursors into highly substituted, structurally diverse and functionally concentrated products.