104316-32-7

Basic information

• Product Name: 4-chlorophenyl pentanoate
• Synonyms: 4-chlorophenyl pentanoate
• CAS NO: 104316-32-7
• Molecular Formula: C₁₁H₁₃ClO₂
• Molecular Weight: 212.67272
• Mol File: 104316-32-7.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-chlorophenyl pentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chlorophenyl pentanoate(104316-32-7)
• EPA Substance Registry System: 4-chlorophenyl pentanoate(104316-32-7)

Safety Data

• Hazardous Substances Data: 104316-32-7(Hazardous Substances Data)

Upstream product

• 542-69-8 1-iodo-butane 
• 201230-82-2 carbon monoxide 
• 106-48-9 4-chloro-phenol 
• 110-62-3 pentanal 

Downstream Products

• 209462-25-9 1-(5-chloro-2-hydroxy-phenyl)-pentan-1-one 
• 138457-63-3 (R)-1-phenylethyl pentanoate 
• 1342259-85-1 (R)-1-(3,4-dimethylphenyl)ethyl valerate 
• 1342259-84-0 (R)-1-(2,4-dimethylphenyl)ethyl valerate 
• 1342259-89-5 (R)-1-(3-chlorophenyl)ethyl valerate 
• 1342259-87-3 (R)-1-(4-chlorophenyl)ethyl valerate 
• 1342259-91-9 (R)-1-(3,4-dimethoxyphenyl)ethyl valerate 
• 1342259-88-4 (R)-1-(2-chlorophenyl)ethyl valerate 
• 1342259-81-7 (R)-1-(2-methylphenyl)ethyl valerate 
• 1342259-83-9 (R)-1-(3,5-dimethylphenyl)ethyl valerate 
• 1342259-86-2 (R)-1-(2,3-dimethylphenyl)ethyl valerate 
• 134615-31-9 (R)-1-(4-bromophenyl)ethyl valerate 
• 1449744-83-5 C₁₅H₂₂O₂ 
• 1528751-77-0 C₁₃H₁₇Cl₂NO 

Relevant articles and documents

Photoinduced Specific Acylation of Phenolic Hydroxy Groups with Aldehydes

A convenient method is reported to specifically acylate phenolic hydroxyl groups through a radical pathway. When a mixture of an aldehyde and a phenol in ethyl acetate is irradiated with blue light in the presence of iridium and nickel bromide catalysts at ambient temperature, phenoxyl and acyl radicals are transiently generated in situ and cross-couple to furnish an ester. Aliphatic hydroxy groups remain untouched under the reaction conditions.

Rhodium-Catalyzed Carbonylative Coupling of Alkyl Halides with Phenols under Low CO Pressure

A rhodium-catalyzed carbonylative transformation of alkyl halides under low pressure of CO has been developed. This robust catalyst system allows using phenols as the carbonylative coupling partner and, meanwhile, exhibits high functional group tolerance and good chemoselectivity. Substrates even with a large steric hindrance group or multiple reaction sites can be selectively converted into the desired products in good to excellent yields. A gram-scale experiment was performed and delivered an almost quantitative amount of the product. Control experiments were performed as well, and a possible reaction mechanism is proposed.