83491-06-9

Basic information

• Product Name: Dodecanoic acid, 4-chlorophenyl ester
• CAS NO: 83491-06-9
• Molecular Formula: C18H27ClO2
• Molecular Weight: 310.864
• Mol File: 83491-06-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Dodecanoic acid, 4-chlorophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Dodecanoic acid, 4-chlorophenyl ester(83491-06-9)
• EPA Substance Registry System: Dodecanoic acid, 4-chlorophenyl ester(83491-06-9)

Safety Data

• Hazardous Substances Data: 83491-06-9(Hazardous Substances Data)

Upstream product

• 74448-92-3 4-(4'-chlorophenoxy)benzonitrile 
• 102020-26-8 dodecanethioic acid S-p-tolyl ester 
• 112-16-3 n-dodecanoyl chloride 
• 106-48-9 4-chloro-phenol 
• 143-07-7 lauric acid 

Downstream Products

• 143-07-7 lauric acid 
• 106-48-9 4-chloro-phenol 
• 24573-38-4 4-chlorophenolate 
• 115-05-9 laurate anion 

Relevant articles and documents

Rhodium-Catalyzed Synthesis of Unsymmetric Di(heteroaryl) Sulfides Using Heteroaryl Ethers and S-Heteroaryl Thioesters via Heteroarylthio Exchange

Unsymmetric di(heteroaryl) sulfides were synthesized by a rhodium-catalyzed heteroarylthio exchange reaction of heteroaryl aryl ethers and S-(heteroaryl) thioesters. The reaction has broad applicability, giving diverse unsymmetric di(heteroaryl) sulfides containing five- and six-membered heteroarenes. No base is required in this reaction, which has been developed by the judicious design of organic substrates.

the Effect of Hydrophobic-Lipophilic Interactions on Chemical Reactivity. 1. New Evidence for Intermolecular Aggregation and Self-Coiling

The hydrolytic behavior of 21 para-substituted phenyl esters of n-alkanoic acids (n-X) with various chain lengths in 60:40 (Φ=0.60), 50:50 (Φ=0.50), and 40:60 v/v (Φ=0.40) Me2SO-H2O mixtures was studied.Four new sets of experimental results which include departure from Hammett correlation for N-hexadecanoates (16-X), substantial differences in activation parameters, and effects of amylose on the kinetic parameters and on the activation parameters are presented along lines of reasoning mentioned by previous authors.These data establish that the aggregation and self-coiling of the n-alkanoate chain actually exist under experimental conditions.