96818-18-7

Basic information

• Product Name: Benzenebutanoic acid, 2,4-dimethoxy-
• CAS NO: 96818-18-7
• Molecular Formula: C12H16O4
• Molecular Weight: 224.257
• Mol File: 96818-18-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenebutanoic acid, 2,4-dimethoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenebutanoic acid, 2,4-dimethoxy-(96818-18-7)
• EPA Substance Registry System: Benzenebutanoic acid, 2,4-dimethoxy-(96818-18-7)

Safety Data

• Hazardous Substances Data: 96818-18-7(Hazardous Substances Data)

Upstream product

• 151-10-0 1,3-Dimethoxybenzene 
• 108-30-5 succinic acid anhydride 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 51114-95-5 (E)-4-(3’,5’-dimethoxyphenyl)but-3-enoic acid 
• 14617-06-2 3-(2',4'-dimethoxybenzoyl)propionic acid 

Downstream Products

• 96818-22-3 4-(2,4-Dimethoxy-phenyl)-butyryl chloride 
• 156868-45-0 2,4-methoxy-α,α-dimethylbenzenebutanol 
• 872832-59-2 (+/-)-1-benzyloxy-7-methoxy-1-azaspiro[5.5]undeca-7,10-diene-2,9-dione 
• 100388-20-3 4-(5-bromo-2,4-dimethoxy-phenyl)-butyric acid 
• 107153-52-6 4-(2,4-dimethoxy-phenyl)-butan-1-ol 
• 106379-77-5 5-(2,4-dimethoxy-phenyl)-pentan-2-ol 
• 109934-45-4 4-nitro-benzoic acid-[4-(2,4-dimethoxy-phenyl)-butyl ester] 

Relevant articles and documents

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Making use of the Hauser-Kraus annulation as a key step, the first total synthesis of tetarimycin A has been accomplished in a highly convergent and operationally simple manner. Preliminary SAR not only validated that tetarimycin A exhibited potent activi

Intramolecular Friedel-Crafts Acylation Reaction Promoted by 1,1,1,3,3,3-Hexafluoro-2-propanol

Simple dissolution of an arylalkyl acid chloride in 1,1,1,3,3,3-hexafluoro-2-propanol promotes an intramolecular Friedel-Crafts acylation without additional catalysts or reagents. This reaction is operationally trivial in both execution and product isolation (only requiring concentration followed by purification) and accommodates a broad range of substrates. Preliminary studies that bear upon potential reaction mechanisms are reported.