27364-22-3

Basic information

• Product Name: 4-HYDROXY-1-(4-METHOXYPHENYL)-1-BUTANONE
• Synonyms: 4-HYDROXY-1-(4-METHOXYPHENYL)-1-BUTANONE
• CAS NO: 27364-22-3
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.23
• Mol File: 27364-22-3.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-HYDROXY-1-(4-METHOXYPHENYL)-1-BUTANONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-HYDROXY-1-(4-METHOXYPHENYL)-1-BUTANONE(27364-22-3)
• EPA Substance Registry System: 4-HYDROXY-1-(4-METHOXYPHENYL)-1-BUTANONE(27364-22-3)

Safety Data

• Hazardous Substances Data: 27364-22-3(Hazardous Substances Data)

Upstream product

• 96-48-0 4-butanolide 
• 100-66-3 methoxybenzene 
• 86119-84-8 phosphoric acid 
• 1191-99-7 2,3-dihydro-2H-furan 
• 696-62-8 para-iodoanisole 
• 3153-44-4 4-(4-methoxy-phenyl)-4-oxo-butyric acid 
• 398142-14-8 4-(4-methoxy-phenyl)-4-pentenoic acid 
• 127047-19-2 4-(4-methoxyphenyl)pent-4-en-1-ol 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 58688-30-5 α-(4-methoxybenzoyl)-γ-butyrolactone 
• 100-07-2 4-methoxy-benzoyl chloride 
• 164171-80-6 1-(4-methoxyphenyl)cyclobutan-1-ol 
• 121-98-2 methyl 4-methoxybenzoate 
• 107840-88-0 2,2-simethyl-1,3-oxathiane 3,3-dioxide 

Downstream Products

• 126135-42-0 (R)-(+)-γ-(p-Methoxyphenyl)-γ-butyrolactone 
• 128994-28-5 (S)-(-)-γ-(p-Methoxyphenyl)-γ-butyrolactone 
• 215667-87-1 4-iodo-1-(4-methoxyphenyl)-1-butanone 
• 56139-60-7 1-(4-Methoxyphenyl)-1,4-butandion 

Relevant articles and documents

Preparation of aromatic γ-hydroxyketones by means of Heck coupling of aryl halides and 2,3-dihydrofuran, catalyzed by a palladium(ii) glycine complex under microwave irradiation

A series of aromatic γ-hydroxyketones were prepared by means of Heck coupling reaction of aryl halides and 2,3-dihydrofuran, catalyzed by PdCl2·Gly2 and under microwave irradiation. This synthetic transformation involves the formation of an aryl-dihydrofuranoic intermediate, followed by an unusual opening of the heterocycle promoted by a water molecule and the formation of the ketone carbonyl function through keto-enol tautomerism. This journal is

Cobalt-catalyzed oxidative cyclization of gem-disubstituted conjugated alkenols

Aryl gem-disubstituted conjugated alkenols underwent oxidative cyclization affording 2,5,5-trisubstituted tetrahydrofurans in reasonable yields and good diastereoselectivities using the reductive termination variation of the Mukaiyama aerobic oxidative reaction. Under oxidative termination, the same alkenols produced diols and ketonic by-products via the double hydration and beta-scission competing pathways. Furthermore, the differences in alkenol reactivity under the reductive and oxidative termination conditions were investigated.

Enantioselective ketone hydroacylation using noyori's transfer hydrogenation catalyst

An enantioselective ketone hydroacylation enables the direct preparation of lactones from keto alcohols. The alcohol is oxidized in situ to an aldehyde, obviating the need to prepare sensitive keto aldehyde substrates. Noyori's asymmetric transfer hydroge