40782-53-4

Basic information

• Product Name: 4-OCTYLOXYBENZOYL CHLORIDE
• Synonyms: 4-OCTYLOXYBENZOYL CHLORIDE;4-N-OCTYLOXYBENZOYL CHLORIDE;P-(OCTYLOXY)BENZOYL CHLORIDE;4-(Octyloxy)benzoic acid chloride
• CAS NO: 40782-53-4
• Molecular Formula: C₁₅H₂₁ClO₂
• Molecular Weight: 268.78
• Mol File: 40782-53-4.mol
• Article Data: 157

Chemical Properties

• Boiling Point: 369.1 °C at 760 mmHg
• Flash Point: 136 °C
• Appearance: /
• Density: 1.052 g/cm³
• Vapor Pressure: 1.21E-05mmHg at 25°C
• Refractive Index: 1.503
• CAS DataBase Reference: 4-OCTYLOXYBENZOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-OCTYLOXYBENZOYL CHLORIDE(40782-53-4)
• EPA Substance Registry System: 4-OCTYLOXYBENZOYL CHLORIDE(40782-53-4)

Safety Data

• Hazardous Substances Data: 40782-53-4(Hazardous Substances Data)

Usage

General Description

4-Octyloxybenzoyl chloride is a chemical compound with the molecular formula C15H21ClO2. It is a benzoyl chloride derivative that is commonly used in organic synthesis as a reactive intermediate. 4-OCTYLOXYBENZOYL CHLORIDE is a colorless to pale yellow liquid with a sharp, pungent odor. It is highly reactive and can hydrolyze in the presence of moisture. 4-Octyloxybenzoyl chloride is used in the production of pharmaceuticals, agrochemicals, and other organic compounds, where it is utilized as an acylating agent in various reactions. Its reactivity and versatility make it a valuable building block in the synthesis of a wide range of organic compounds.

InChI:InChI=1/C15H21ClO2/c1-2-3-4-5-6-7-12-18-14-10-8-13(9-11-14)15(16)17/h8-11H,2-7,12H2,1H3

Upstream product

• 111-83-1 1-bromo-octane 
• 111-87-5 octanol 
• 5519-23-3 p-decyloxybenzoic acid 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 99-96-7 4-hydroxy-benzoic acid 
• 2493-84-7 p-octyloxybenzoic acid 
• 55546-15-1 propylene glycol 1-O-pentyl ether 
• 629-27-6 1-Iodooctane 
• 16782-08-4 sel de potassium de l'acide p-hydroxybenzoique 
• 72885-31-5 4-octyloxy-benzoic acid ethyl ester 
• 99-76-3 methyl 4-hydroxylbenzoate 
• 62435-37-4 methyl 4-(octyloxy)benzoate 

Downstream Products

• 112949-76-5 4-octyloxy-benzoic acid-(3-dimethylamino-1,2-dimethyl-propyl ester) 
• 24707-08-2 1,4-Bicyclo<2,2,2>oktylen-di-p-oktoxy-benzoat 
• 72997-70-7 2-(4-octyloxy-phenyl)-5-phenyl-thiazole 
• 72997-52-5 5-(4-methoxy-phenyl)-2-(4-octyloxy-phenyl)-thiazole 
• 72997-66-1 2-(4-octyloxy-phenyl)-5-(4-propoxy-phenyl)-thiazole 
• 72997-43-4 4-octyloxy-N-[2-oxo-2-(4-propoxy-phenyl)-ethyl]-benzamide 
• 50649-56-4 4-pentylphenylester of 4-octyloxybenzoic acid 
• 121586-77-4 3,4-Bis-(4-octyloxy-benzoyloxy)-benzoic acid 
• 61945-84-4 4(4-Octyloxybenzoyloxy)-4'-cyanoazobenzol 

Relevant articles and documents

Simple and efficient chiral dopants to induce blue phases and their optical purity effects on the physical properties of blue phases

Blue phases (BPs) have received considerable attention as light shutters in the next generation of liquid crystal (LC) displays. However, no simple and efficient chiral dopant for induction of BPs of commercially available rodlike LC compounds has been re

Synthesis and characterization of novel rod-like ester-based liquid crystalline homologous series: Effect of tert-butyl tail on mesomorphism

A new rod-like homologous series consisting twelve compounds with central ester linkage and terminal tert-butyl group, tert-butyl [4-(4’-n-alkoxybenzoyloxy)benzoates] has been synthesized and characterized through standard spectroscopic techniques like UV, FT-IR, 1HNMR, DSC, POM, and XRD. Methoxy and ethoxy derivatives are nonmesogenic. Nematic mesophase commences as enantiotropy from propyloxy derivative and persists up to the octadecyloxy derivatives. Smectic A mesophase commences as monotropy from propyloxy to the octadecyloxy derivatives. The mesomorphic properties of present series are compared with other structurally related series to evaluate the effect of terminal tert-butyl group on mesomorphism. Two derivatives are subjected to in?vitro antimicrobial activity.

Synthesis of glycerolipids containing simple linear acyl chains or aromatic rings and evaluation of their Mincle signaling activity

Mincle, expressed in activated phagocytes, recognizes the lipid ligand to activate the innate immune system. We have synthesized glycerol derivatives possessing simple alkyl chains or aromatic rings and elucidated their structure-activity relationships us