31526-44-0

Basic information

• Product Name: 4-p-Anisoyl-3.3-dimethylbuttersaeure
• Synonyms: 4-p-Anisoyl-3.3-dimethylbuttersaeure
• CAS NO: 31526-44-0
• Molecular Weight: 250.295
• Mol File: 31526-44-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-p-Anisoyl-3.3-dimethylbuttersaeure(CAS DataBase Reference)
• NIST Chemistry Reference: 4-p-Anisoyl-3.3-dimethylbuttersaeure(31526-44-0)
• EPA Substance Registry System: 4-p-Anisoyl-3.3-dimethylbuttersaeure(31526-44-0)

Safety Data

• Hazardous Substances Data: 31526-44-0(Hazardous Substances Data)

Upstream product

• 4160-82-1 3,3-dimethylglutaric anhydride 
• 100-66-3 methoxybenzene 
• 108-55-4 glutaric anhydride, 

Downstream Products

• 135312-40-2 3,3-dimethyl-5-(4-hydroxyphenyl)-5-oxopentanoic acid 
• 119348-28-6 1-{4-[(4-acetyl-3-hydroxy-2-propylphenyl)methoxy]phenyl}-3,3-dimethyl-4-(1H-tetrazol-5-yl)-1-butanone 
• 119348-36-6 4-[(4-Acetyl-3-hydroxy-2-propylphenyl)methoxy]-β,β-dimethyl-δ-oxobenzenepentanoic acid, ethyl ester 
• 119348-47-9 1-{4-[(4-acetyl-3-hydroxy-2-ethylphenyl)methoxy]phenyl}-3,3-dimethyl-4-(1H-tetrazol-5-yl)-1-butanone 
• 119348-51-5 4-[(4-Acetyl-2-ethyl-3-hydroxyphenyl)methoxy]β,β-dimethyl-δ-oxobenzenepentanoic acid, ethyl ester 
• 135312-28-6 5-<4-<<(4-acetyl-3-hydroxy-2-propylphenyl)methyl>thio>phenyl>-3,3-dimethyl-5-oxopentanoic acid 
• 119348-29-7 4-[(4-acetyl-3-hydroxy-2-propylphenyl)methoxy]-β,β-dimethyl-δ-oxobenzenepentanoic acid 
• 119348-31-1 5-[4-(4-Acetyl-3-hydroxy-2-propyl-benzyloxy)-phenyl]-3,3-dimethyl-5-oxo-pentanenitrile 
• 119348-30-0 5-<4-<(4-acetyl-2-ethyl-3-hydroxyphenyl)methoxy>phenyl>-3,3-dimethyl-5-oxopentanoic acid 
• 119348-32-2 5-[4-(4-Acetyl-2-ethyl-3-hydroxy-benzyloxy)-phenyl]-3,3-dimethyl-5-oxo-pentanenitrile 
• 119348-66-2 3,3-dimethyl-5-(4-hydroxyphenyl)-5-oxopentanoic acid ethyl ester 
• 135312-46-8 3,3-dimethyl-5-oxo-5-(4-mercaptophenyl)pentanoic acid 
• 135312-41-3 3,3-dimethyl-5-(4-hydroxyphenyl)-5-oxopentanenitrile 
• 135312-42-4 5-(4-Hydroxy-phenyl)-3,3-dimethyl-5-oxo-pentanenitrile 

Relevant articles and documents

Enantioselective Bromolactonization of Deactivated Olefinic Acids

A novel enantioselective bromolactonization of α,β-unsaturated ketones using bifunctional amino-urea catalysts has been developed. The scope of the reaction is evidenced by 23 examples of halolactones bearing various functionalities with up to 99% yield a