105705-43-9

Basic information

• Product Name: Benzoic acid, 2,4-dimethoxy-6-(3-oxopentyl)-
• CAS NO: 105705-43-9
• Molecular Formula: C14H18O5
• Molecular Weight: 266.294
• Mol File: 105705-43-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2,4-dimethoxy-6-(3-oxopentyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2,4-dimethoxy-6-(3-oxopentyl)-(105705-43-9)
• EPA Substance Registry System: Benzoic acid, 2,4-dimethoxy-6-(3-oxopentyl)-(105705-43-9)

Safety Data

• Hazardous Substances Data: 105705-43-9(Hazardous Substances Data)

Upstream product

• 616-25-1 1-Penten-3-ol 
• 91-52-1 2,4 dimethoxybenzoic acid 
• 105705-33-7 diethyl 2-(2-bromo-3,5-dimethoxybenzyl)propane-1,3-dione 
• 105705-35-9 2-(2-bromo-3,5-dimethoxybenzyl)propane-1,3-dioic acid 
• 105705-39-3 1-(2-bromo-3,5-dimethoxyphenyl)pentan-3-one 
• 105705-37-1 3-(2-bromo-3,5-dimethoxyphenyl)propanoic acid 
• 105705-19-9 3-(2-Bromo-3,5-dimethoxy-phenyl)-propionyl chloride 
• 105705-31-5 2-bromo-3,5-dimethoxybenzyl chloride 
• 124-38-9 carbon dioxide 
• 105705-41-7 1-(2-bromo-3,5-dimethoxyphenyl)-3,3-diethoxypentane 

Downstream Products

• 35578-70-2 miriquidic acid 
• 105705-18-8 benzyl miriquidate 
• 35583-00-7 2-hydroxy-4-methoxy-6-(3-oxopentyl)benzoic acid 

Relevant articles and documents

Ruthenium-Catalyzed C-H Functionalization of Benzoic Acids with Allyl Alcohols: A Controlled Reactivity Switch between C-H Alkenylation and C-H Alkylation Pathways

A highly selective and switchable ruthenium-catalyzed ortho C-H alkylation and C-H alkenylation of benzoic acids with allyl alcohols is reported. A complete switch in selectivity is achieved upon tuning the reactivity of the organometallic intermediate in the carboxylate-directed C-H activation to provide access to highly useful motifs such as 2-alkylbenzoic acids and phthalides.