25800-30-0

Basic information

• Product Name: propyl 4-chlorobenzoate
• Synonyms: Propyl 4-chlorobenzoate
• CAS NO: 25800-30-0
• Molecular Formula: C₁₀H₁₁ClO₂
• Molecular Weight: 198.6461
• Mol File: 25800-30-0.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 256.3°C at 760 mmHg
• Flash Point: 116.8°C
• Density: 1.152g/cm³
• Vapor Pressure: 0.0155mmHg at 25°C
• Refractive Index: 1.517
• CAS DataBase Reference: propyl 4-chlorobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: propyl 4-chlorobenzoate(25800-30-0)
• EPA Substance Registry System: propyl 4-chlorobenzoate(25800-30-0)

Safety Data

• Hazardous Substances Data: 25800-30-0(Hazardous Substances Data)

Upstream product

• 98-56-6 4-chlorobenzotrifluoride 
• 71-23-8 propan-1-ol 
• 27704-37-6 2,2,2-trichloro-1-(4-chlorophenyl)ethanone 
• 104-88-1 4-chlorobenzaldehyde 
• 56741-11-8 methylidene di(4-chlorobenzoate) 
• 925-90-6 ethylmagnesium bromide 
• 201230-82-2 carbon monoxide 
• 99-91-2 para-chloroacetophenone 
• 195062-61-4 4-chlorophenylboronic acid pinacol ester 
• 74-11-3 para-chlorobenzoic acid 
• 873-76-7 para-Chlorobenzyl alcohol 
• 106-94-5 propyl bromide 
• 124-38-9 carbon dioxide 
• 21700-74-3 (p-chlorophenyl)triethoxysilane 

Downstream Products

• 94-12-2 risocaine 

Relevant articles and documents

Synthesis and characterization of stable ZnO nanoparticles using imidazolium-based ionic liquids and their applications in esterification reaction

ZnO nanoparticles have been synthesized from zinc acetate using 1-octyl-3-methylimidazolium hexafluorophosphate as capping agent under microwave irradiation condition in a very short period of time and characterized using UV-visible spectroscopy, powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy and NH3-TPD analysis. The ZnO NPs have been used as a solid reusable acid catalyst for esterification of carboxylic acids with alcohols.

Oxidation of benzaldehydes to benzoate esters using household bleach and sodium iodide in alcohol solvents

Various substituted benzaldehydes were converted into benzoate esters with household bleach and sodium iodide in an alcohol solvent. The reaction works best with methanol. Only 4-chlorobenzaldehyde, 3-nitrobenzaldehyde, and 4-nitrobenzaldehyde reacted completely with 1-propanol under these conditions. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.] Copyright

Facile esterification of carboxylic acid using amide functionalized benzimidazolium dicationic ionic liquids

Herein, we report the synthesis of a new series of amide functionalized dicationic benzimidazolium based ionic liquids (DBimILs) and appraised their efficacy towards perceptive esterification of carboxylic acids with alkyl/allyl/aryl halides in presence of triethylamine. The amide groups present in this new series of DBimILs are expected to form hydrogen bonding with the carboxylic acids and this could facilitate the esterification reactions under mild conditions devoid of any added catalyst or organic solvent. The plausible mechanism for the enhanced catalytic activity in presence of this new series of ILs has been proposed. The corresponding alkyl/allyl/aryl esters isolated from this reaction were of high purity after simple extraction, which wipe out the necessity for further purification. This protocol addresses clean methodology and the efficient recyclability as well as reusability of the catalyst.