138320-27-1

Basic information

• Product Name: 2-(2-ForMylphenoxy)hexanoic acid
• Synonyms: 2-(2-ForMylphenoxy)hexanoic acid
• CAS NO: 138320-27-1
• Molecular Formula: C₁₃H₁₆O₄
• Molecular Weight: 236.26374
• Mol File: 138320-27-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 394.6±17.0 °C(Predicted)
• Appearance: /
• Density: 1.165±0.06 g/cm3(Predicted)
• PKA: 3.09±0.10(Predicted)
• CAS DataBase Reference: 2-(2-ForMylphenoxy)hexanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-ForMylphenoxy)hexanoic acid(138320-27-1)
• EPA Substance Registry System: 2-(2-ForMylphenoxy)hexanoic acid(138320-27-1)

Safety Data

• Hazardous Substances Data: 138320-27-1(Hazardous Substances Data)

Usage

General Description

2-(2-Formylphenoxy)hexanoic acid is a chemical compound consisting of a hexanoic acid molecule with a 2-Formylphenoxy group attached to the 2-position. It is commonly used as a building block in organic chemistry and can be used in the synthesis of various pharmaceuticals, agrochemicals, and materials. The compound may also have potential biological and pharmacological properties, making it a subject of interest in medicinal chemistry research. 2-(2-Formylphenoxy)hexanoic acid is a versatile chemical with potential applications in various industries, making it a valuable compound for scientific and commercial purposes.

Upstream product

• 5445-19-2 methyl 2-bromohexanoate 
• 90-02-8 salicylaldehyde 
• 138320-26-0 methyl 2-(2-formylphenoxy)hexanoate 

Downstream Products

• 4265-27-4 2-n-butylbenzo[b]furan 
• 97025-19-9 2-(o-carboxyphenoxy)hexanoic acid 
• 19774-82-4 amiodarone hydrochloride 
• 52490-15-0 2-n-Butyl-3-(4-hydroxy-benzoyl)-benzofuran 
• 1951-26-4 2-n-butyl-3-(3',5'-diiodo-4'-hydroxybenzoyl)benzofuran 
• 83790-87-8 2-n-butyl 3-(4-methoxy benzoyl)-benzofuran 
• 335153-21-4 2-(2-formyl-4-nitrophenoxy)hexanoic acid 
• 95486-76-3 1-[3-(2-butylbenzofuranyl)]-2-(4-hydroxyphenyl)ethanone 
• 199725-34-3 1-[3-(2-butylbenzofuranyl)]-2-phenylethanone 
• 94968-16-8 1-<3-(2-butylbenofuranyl)>-2-(4-methoxyphenyl)ethanone 

Relevant articles and documents

Preparation method of amiodarone hydrochloride intermittent

The invention belongs to the field of medicine synthesis, and relates to a preparation method of an amiodarone hydrochloride intermittent. The method is characterized by including the following stepsthat 1, under an alkaline condition, in the presence of a phase transfer catalyst, a compound 1 and a compound 2 are subjected to nucleophilic substitution reaction to obtain a compound 3; 2, under analkaline condition, the compound 3 is hydrolyzed to generate a compound 4; 3, the compound 4 is subjected to intramolecular aldol condensation, decarboxylation and dehydration to obtain a compound 5;4, a compound 6 and thionyl chloride are subjected to heating reaction to obtain a compound 7; 5, under the presence of lewis acid, the compound 5 and the compound 7 are subjected to friede-crafts acylation reaction to obtain a compound 8; 6, under the presence of lewis acid, the compound 8 is subjected to demethylation to generate a compound 9, namely the amiodarone hydrochloride intermittent 2-butyl-3-(4-hydroxybenzoyl)benzofuran. The preparation method of the amiodarone hydrochloride intermittent has the advantages of being short in reaction time, high in product purity and high in yield,and the amiodarone hydrochloride intermittent is suitable for large-scale industrial production.

Intermediates for making a bezofuran or benzothiophene derivative nitrated in position 5 and uses thereof

The invention concerns novel nitroaromatic compounds of general formula (I′) wherein: R, R′1, R2, Z and n are as defined in claim 1. The invention also concerns a method for preparing nitroaromatic compounds nitrated in position 4. The invention further c

Synthesis of 2-Phenoxyhexanal and 2-(o-Formylphenoxy)Hexanoic Acid and Its Derivatives

The paper describes the synthesis of 2-phenoxyhexanal and 2-(o-formylphenoxy)hexanoic acid and its derivatives which are intermediate compounds in the synthesis of new heterocyclic compounds.Key words: 2-phenoxyhexanal, 2-phenoxyhexanoic acid derivatives, 2-butylbenzofurane