25173-36-8

Basic information

• Product Name: 3-M-TOLYLOXY-PROPIONIC ACID
• Synonyms: 3-(3-Methylphenoxy)propionic Acid
• CAS NO: 25173-36-8
• Molecular Formula: C₁₀H₁₂O₃
• Molecular Weight: 180.21
• Mol File: 25173-36-8.mol
• Article Data: 6

Chemical Properties

• Melting Point: 105 °C
• Boiling Point: 295.5°C at 760 mmHg
• Flash Point: 114.7°C
• Appearance: /
• Density: 1.145±0.06 g/cm3(Predicted)
• Vapor Pressure: 0.000687mmHg at 25°C
• PKA: 4.24±0.10(Predicted)
• CAS DataBase Reference: 3-M-TOLYLOXY-PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-M-TOLYLOXY-PROPIONIC ACID(25173-36-8)
• EPA Substance Registry System: 3-M-TOLYLOXY-PROPIONIC ACID(25173-36-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 25173-36-8(Hazardous Substances Data)

Usage

General Description

3-M-TOLYLOXY-PROPIONIC ACID, also known as 3-Methylphenyl propionic acid, is a type of chemical compound which belongs to the class of organic compounds known as benzenoids. These are aromatic compounds containing one or more benzene rings. This specific compound has not been widely researched or used, and little information is available on its properties or potential applications. Like other organic compounds, it could potentially be used in a wide range of industrial applications like pharmaceuticals, dyes, detergents, and polymers. However, further research is needed to confirm its specific properties and potential uses.

InChI:InChI=1/C10H12O3/c1-8-3-2-4-9(7-8)13-6-5-10(11)12/h2-4,7H,5-6H2,1H3,(H,11,12)/p-1

Upstream product

• 57-57-8 β-Propiolactone 
• 3019-89-4 sodium 3-methylphenoxide 
• 13030-21-2 3-(m-methylphenoxy)propan-1-ol 
• 25268-06-8 3-(m-tolyloxy)propionitrile. 
• 108-39-4 3-methyl-phenol 
• 107-13-1 acrylonitrile 
• 107-94-8 chloropropionic acid 
• 106-44-5 p-cresol 

Downstream Products

• 18385-69-8 7-methylchroman-4-one 
• 13629-89-5 3-m-Tolyloxy-propionsaeure-vinylester 
• 91634-24-1 3-<3-Carboxy-phenoxy>-propionsaeure 
• 90921-09-8 acide chromannone-4 carboxylique-7 
• 5751-51-9 7-methyl-4H-benzopyran-4-one 
• 91880-46-5 3-<3-Carbamoyl-phenoxy>-propionamid 
• 94112-90-0 3-<3-Aethoxycarbonyl-phenoxy>-propionsaeure-aethylester 
• 915923-06-7 C₁₁H₁₃N₃OS 
• 18385-68-7 5-methyl-2,3-dihydrochromen-4-one 

Relevant articles and documents

Acid activated montmorillonite K-10 mediated intramolecular acylation: Simple and convenient synthesis of 4-chromanones

3-Aryloxyproionic acids undergo intramolecular cyclization in the presence of AA.Mont.K-10 in toluene under reflux for 30–45 min in good to excellent yields. Phenyl ring bearing various substituents at the ortho, meta, para positions undergo this cyclization reaction. This method involves simple work up and amenable for large scale preparations. The heterogeneous acid treated catalyst can be regenerated and used for up to three cycles with minimum loss of activity.

Preparation method of oxygen heterocyclic compound

The invention discloses a preparation method of an oxygen heterocyclic compound 4-hydroxyl-5-methyl-3,4-dihydro-2H-chromene-4-carboxylic acid. With 4-methylphenol as a start raw material, a target product is prepared by condensation, ring closing, cyaniding, TMS removal and hydrolysis. The compound is an important pharmaceutical intermediate.

SYNTHESIS OF PROPYL PHENOXY ETHERS AND USE AS DELIVERY AGENTS

The present invention provides propyl phenoxy ether compounds and pharmaceutically acceptable salts thereof, compositions containing the same and one or more active agents, and methods of administering active agents with the same. The delivery agents of the present invention are well suited for forming non-covalent mixtures with active agents for oral, iπtracolonic, pulmonary, and other routes of administration to animals.