150272-46-1

Basic information

• Product Name: 3-phenyl-1-propyl p-trifluoromethylbenzoate
• Synonyms: 3-phenyl-1-propyl p-trifluoromethylbenzoate
• CAS NO: 150272-46-1
• Molecular Weight: 308.3
• Mol File: 150272-46-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-phenyl-1-propyl p-trifluoromethylbenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-1-propyl p-trifluoromethylbenzoate(150272-46-1)
• EPA Substance Registry System: 3-phenyl-1-propyl p-trifluoromethylbenzoate(150272-46-1)

Safety Data

• Hazardous Substances Data: 150272-46-1(Hazardous Substances Data)

Upstream product

• 122-97-4 3-Phenyl-1-propanol 
• 25753-16-6 4-(trifluoromethyl)benzoic anhydride 
• 501-52-0 3-Phenylpropionic acid 
• 299203-18-2 1-triphenylmethoxy-3-phenylpropane 
• 329-15-7 4-trifluoromethyl-phenyl acetyl chloride 
• 14629-60-8 trimethyl(3-phenylpropoxy)silane 
• 37170-49-3 trimethylsilyl 2,2-dimethylpropionate 

Relevant articles and documents

An Effective Use of Benzoic Anhydride and Its Derivatives for the Synthesis of Carboxylic Esters and Lactones: A Powerful and Convenient Mixed Anhydride Method Promoted by Basic Catalysts

Various carboxylic esters are obtained at room temperature in excellent yields with high chemoselectivities from nearly equimolar amounts of carboxylic acids and alcohols using 2-methyl-6-nitrobenzoic anhydride with triethylamine by the promotion of a basic catalyst such as 4-(dimethylamino)pyridine. A variety of lactones are also prepared in high yields at room temperature from the corresponding ω-hydroxycarboxylic acids with use of 2-methyl-6-nitrobenzoic anhydride in the presence of 4-(dimethylamino)pyridine. A similar reaction occurs with triethylamine when using a catalytic amount of 4-(dimethylamino)pyridine 1-oxide as an effective promoter for the intramolecular condensation reaction. These methods are successfully applied to the synthesis of erythro-aleuritic acid lactone and an eight-membered-ring lactone moiety of octalactins A and B. The efficiency of the cyclizations is compared to those of other reported lactonizations.

A convenient one-step method for the deprotection and esterification of triphenylmethyl ethers

We have discovered a simple one-pot procedure to convert trityl ethers into esters, using the corresponding acid chloride as the only reagent. (C) 2000 Elsevier Science Ltd.

An Efficient Method for the Preparation of Carboxylic Esters via Mixed Anhydrides by the Promotion of a Catalytic Amount of Lewis Acid

Various carboxylic esters are prepared in excellent yields by the reaction of nearly equimolar amounts of silyl derivatives of carboxylic acids and alcohols with p-trifluoromethylbenzoic anhydride in the presence of a catalytic amount of Lewis acid.