96524-70-8

Basic information

• Product Name: Methyl(p-formylphenyl)acetate
• Synonyms: Methyl(p-formylphenyl)acetate;(4-Formylphenyl)acetic acid methyl ester;4-Formylbenzeneacetic acid methyl ester;Methyl (4-formylphenyl)acetate;Methyl 2-(4-formylphenyl)acetate;Methyl 2-(4-formylphenyl);Benzeneacetic acid, 4-formyl-, methyl ester
• CAS NO: 96524-70-8
• Molecular Formula: C₁₀H₁₀O₃
• Molecular Weight: 178.1846
• Mol File: 96524-70-8.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 285℃
• Flash Point: 124℃
• Appearance: /
• Density: 1.157
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: Methyl(p-formylphenyl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: Methyl(p-formylphenyl)acetate(96524-70-8)
• EPA Substance Registry System: Methyl(p-formylphenyl)acetate(96524-70-8)

Safety Data

• Hazardous Substances Data: 96524-70-8(Hazardous Substances Data)

Usage

Description

Methyl(p-formylphenyl)acetate, with the molecular formula C11H12O3, is an ester, a type of organic compound formed by the reaction of a carboxylic acid and an alcohol. It is known for its sweet, fruity odor and is widely used in the creation of pleasant smells and tastes in various consumer products.

Uses

Used in Fragrance Industry:
Methyl(p-formylphenyl)acetate is used as a flavoring agent and fragrance in consumer products such as perfumes, soaps, and cosmetics. Its fruity scent is utilized to impart a fruity or floral aroma to these products.
Used in Food Industry:
Methyl(p-formylphenyl)acetate is also commonly used in the production of food flavorings. It is considered safe for consumption in small quantities and contributes to enhancing the taste and aroma of various food items.

Upstream product

• 14199-15-6 Methyl 4-hydroxyphenylacetate 
• 73401-74-8 4-hydroxymethylphenylacetic acid 
• 75-36-5 acetyl chloride 
• 101-41-7 benzeneacetic acid methyl ester 
• 7398-42-7 methyl 2-(4-(bromomethyl)phenyl)acetate 
• 13737-36-5 4-bromophenylacetic acid 
• 147283-85-0 (4-Trifluoromethanesulfonyloxy-phenyl)-acetic acid methyl ester 
• 156-38-7 4-hydroxyphenylacetate 
• 52798-01-3 methyl 4-cyanobenzeneacetate 
• 17833-56-6 ester monomethylique de l'acide p-phenylene diacetique 
• 155380-11-3 methyl 4-(hydroxymethyl)phenylacetate 
• 72770-09-3 4-(chloromethyl)-phenylacetic methylester 

Downstream Products

• 854766-05-5 {4-[({3-[3-benzoyl-8-(trifluoromethyl)quinolin-4-yl]phenyl}amino)methyl]phenyl}acetic acid 
• 927187-42-6 (4-{4-[2-(2,4-dichloro-phenoxy)-ethylcarbamoyl]-5-phenyl-isoxazol-3-yl}-phenyl)-acetic acid methyl ester 
• 1305348-96-2 methyl (4-{[3(adamant-1-ylpropyl)amino]methyl}phenyI)acetate 
• 1613414-62-2 methyl 2-(4-(1,3-dioxolan-2-yl)phenyl)acetate 
• 1080008-18-9 methyl 2-(4-((N-(3-(4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl)propyl)-2-(piperidin-1-yl)acetamido)methyl)phenyl)acetate 
• 1080008-44-1 methyl 2-(4-(((3-(4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl)propyl)(3-morpholinopropyl)amino)methyl)phenyl)acetate 
• 1080008-41-8 methyl 2-(4-((N-(3-(4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl)propyl)-3-(piperidin-1-yl)propanamido)methyl)phenyl)acetate 
• 87077-46-1 1-(4-ethyl-phenyl)-2-methyl-propan-2-ol 
• 7398-47-2 methyl 2-(4-(1-hydroxyethyl)phenyl)acetate 
• 950502-41-7 [2-(2,6-dichloro-phenyl)-ethyl]-(4-{[2R-hydroxy-2-(4-hydroxy-2-oxo-2,3-dihydro-benzothiazol-7-yl)-ethylcarbamoyl]-methyl}-benzyl)-carbamic acid tert-butyl ester 

Relevant articles and documents

Chemoselective Deoxygenation of 2° Benzylic Alcohols through a Sequence of Formylation and B(C6F5)3-Catalyzed Reduction

A sequence of formylation and B(C6F5)3-catalyzed reduction of the resulting formate with Et3SiH enables the chemoselective deoxygenation of secondary benzylic alcohols. Primary benzylic and tertiary non-benzylic alcohols are not reduced by this protocol. The formyl group fulfills a double role as activator and self-sacrificing protecting group. The deoxygenation of these formates is fast and can be carried out in the presence of other potentially reducible groups. Neighboring-group participation was found in the deoxygenation of certain diol motifs.

OXADIAZOLONES AS TRANSIENT RECEPTOR POTENTIAL CHANNEL INHIBITORS

The invention relates to compounds of formula (I) and pharmaceutically acceptable salts thereof. In addition, the present invention relates to methods of manufacturing and methods of using the compounds of formula (I) as well as pharmaceutical compositions containing such compounds. The compounds may be useful in treating diseases and conditions mediated by TRPA1, such as pain.

COMPOUNDS HAVING MUSCARINIC RECEPTOR ANTAGONIST AND BETA2 ADRENERGIC RECEPTOR AGONIST ACTIVITY

Compounds of formula (I) described herein act both as muscarinic receptor antagonists and beta2 adrenergic receptor agonists and are useful for the prevention and/or treatment of broncho-obstructive or inflammatory diseases.