23133-74-6

Basic information

• Product Name: 3,5-Dimethoxyphenol acetate
• Synonyms: 3,5-Dimethoxyphenol acetate;Acetic acid 3,5-dimethoxyphenyl ester
• CAS NO: 23133-74-6
• Molecular Formula: C₁₀H₁₂O₄
• Molecular Weight: 196.2
• Mol File: 23133-74-6.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,5-Dimethoxyphenol acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dimethoxyphenol acetate(23133-74-6)
• EPA Substance Registry System: 3,5-Dimethoxyphenol acetate(23133-74-6)

Safety Data

• Hazardous Substances Data: 23133-74-6(Hazardous Substances Data)

Upstream product

• 500-99-2 3,5-dimethoxyphenol 
• 108-24-7 acetic anhydride 
• 75-36-5 acetyl chloride 

Downstream Products

• 316140-47-3 1-acetoxy-2-bromo-3,5-dimethoxy-benzene 
• 60237-54-9 1-(2,4-dimethoxy-6-(methoxymethoxy)phenyl)ethan-1-one 
• 6093-80-7 5,7-dimethoxy-4-methylcoumarin 
• 487-06-9 Limettin 
• 1422444-40-3 C₁₁H₁₁F₃O₄ 
• 1422444-38-9 3,5-dimethoxy-2-(trifluoromethyl)phenyl acetate 
• 90-24-4 2-hydroxy-4,6-dimethoxyacetophenone 
• 316140-43-9 (2'S)-(-)-1'-fluorooct-7'-en-2'-yl 2,4-dimethoxy-6-trifluoromethanesulfonatebenzoate 
• 316140-41-7 1'-fluorooct-7'-en-2'-yl 2,4-dimethoxy-6-trifluoromethanesulfonatebenzoate 
• 316140-34-8 1'-fluorooct-7'-en-2'-yl 2-allyl-4,6-dimethoxybenzoate 
• 316140-44-0 (2'S)-(-)-1'-fluorooct-7'-en-2'-yl 2-allyl-4,6-dimethoxybenzoate 
• 316140-35-9 1'-fluorooct-7'-en-2'-yl 2-hydroxy-4,6-dimethoxybenzoate 
• 316140-42-8 (2'S)-(-)-1'-fluorooct-7'-en-2'-yl 2-hydroxy-4,6-dimethoxybenzoate 
• 121449-70-5 3-bromo-3,5-dimethoxyphenol 

Relevant articles and documents

3,5-DISUBSTITUTED PYRAZOLES USEFUL AS CHECKPOINT KINASE 1 (CHK1) INHIBITORS, AND THEIR PREPARATIONS AND APPLICATIONS

Potent inhibitors of Chk1 have the structure formula (I) below. Pharmaceutical compositions comprising the Chk1 inhibitors, uses thereof and their preparation process.

Rh-Catalyzed Synthesis of Coumarin Derivatives from Phenolic Acetates and Acrylates via C-H Bond Activation

An efficient annulation strategy involving the reaction of phenolic acetates with acrylates in the presence of [Rh2(OAc)4] as catalyst and formic acid as reducing agent, leading to the high yield synthesis of coumarin derivatives, has been developed. The addition of NaOAc as a base increased the yield of the products. The reaction is quite successful for both electron-rich as well as electron-deficient phenolic acetates, affording coumarins with excellent regioselectivity, and proceeds via C-H bond activation proven by deuterium incorporation studies.

Isolation and synthesis of flavonols and comparison of their antioxidant activity

Phytochemical investigation of the leaves of Astragalus beckari yielded four flavonol aglycones, namely kaempferol, quercetin, 5-deoxy kaempferol and fisitin. These isolated compounds were then synthesised in the laboratory using the Algar-Flyn-Oyamad reaction. Antioxidant activity of both the isolated and synthesised flavonoids was compared using the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay method. The isolated flavonoids were found to be more active.