15561-50-9

Basic information

• Product Name: 2-(2,6-dimethoxyphenyl)acetic acid
• Synonyms: 2-(2,6-dimethoxyphenyl)acetic acid
• CAS NO: 15561-50-9
• Molecular Weight: 196.203
• Mol File: 15561-50-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(2,6-dimethoxyphenyl)acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,6-dimethoxyphenyl)acetic acid(15561-50-9)
• EPA Substance Registry System: 2-(2,6-dimethoxyphenyl)acetic acid(15561-50-9)

Safety Data

• Hazardous Substances Data: 15561-50-9(Hazardous Substances Data)

Usage

Chemical class

Phenylalkanoic acids

Uses

Calcium channel blocker, treatment of high blood pressure, angina, and certain heart rhythm disorders

Mechanism of action

Relaxes and widens blood vessels, improves blood flow, lowers blood pressure, and has antiarrhythmic properties

Molecular weight

218.24 g/mol

Upstream product

• 71819-90-4 2-(chloromethyl)-1,3-dimethoxybenzene 
• 3392-97-0 2,6-dimethoxybenzaldehyde 
• 127378-31-8 5-(2,6-dimethoxy-benzylidene)-2-thioxo-thiazolidin-4-one 
• 151-10-0 1,3-Dimethoxybenzene 
• 3166-95-8 2-(2,6-dimethoxyphenyl)acetonitrile 
• 860189-80-6 3-(2,6-dimethoxy-phenyl)-2-thioxo-propionic acid 

Downstream Products

• 1466-76-8 2-6-dimethoxybenzoic acid 
• 659727-84-1 2-(2,6-dimethoxyphenyl)ethanoyl chloride 

Relevant articles and documents

Isoindolone derivatives, their preparation and the pharmaceutical compositions containing them

This invention relates to isoindolone derivatives of general formula (I) in which the radicals R are hydrogen atoms or together form a bond, the symbols R'' are phenyl radicals which can be substituted by a halogen atom or a methyl radical in position 2 or 3, X is an oxygen or sulphur atom or a radical N--R 3, R 3 being H, optionally substituted alkyl or dialkylamino, R 1 is optionally substituted phenyl or cyclohexadienyl, naphthyl or a heterocycle and R 2 is H, halogen, OH, alkyl, amionoalkyl, alkylaminoalkyl, dialkylaminoalkyl, alkoxy, alkylthio, acyloxy, carboxyl, optionally substituted alkoxycarbonyl, benzyloxycarbonyl, amino or acylamino, in their (3aR,7aR) forms or in the (3aRS,7aRS) form or their mixtures, and if appropriate their salts where such exist, and their preparation.The new derivatives according to the invention are particularly valuable as antagonists of substance P. STR1