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
• Article Data: 2

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

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

Downstream Products

• 138457-63-3 (R)-1-phenylethyl pentanoate 
• 98-86-2 acetophenone 
• 1375463-88-9 (R)-N-(1-phenylethyl)pentamide 
• 1449247-99-7 C₁₇H₂₁NO 
• 1528751-77-0 C₁₃H₁₇Cl₂NO 
• 1449744-83-5 C₁₅H₂₂O₂ 
• 134615-31-9 (R)-1-(4-bromophenyl)ethyl valerate 
• 1342259-86-2 (R)-1-(2,3-dimethylphenyl)ethyl valerate 
• 1342259-83-9 (R)-1-(3,5-dimethylphenyl)ethyl valerate 
• 1342259-81-7 (R)-1-(2-methylphenyl)ethyl valerate 
• 1342259-88-4 (R)-1-(2-chlorophenyl)ethyl valerate 
• 1342259-91-9 (R)-1-(3,4-dimethoxyphenyl)ethyl valerate 
• 1342259-87-3 (R)-1-(4-chlorophenyl)ethyl valerate 
• 1342259-89-5 (R)-1-(3-chlorophenyl)ethyl valerate 

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.