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2-(2,6-dimethoxyphenyl)acetic acid is an organic compound with the chemical formula C10H12O4. It is a derivative of acetic acid, featuring a phenyl ring with two methoxy groups at the 2nd and 6th positions, and a carboxyl group at the 2nd position. 2-(2,6-dimethoxyphenyl)acetic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs. It is characterized by its ability to form salts and esters, which can be used in different chemical reactions. The compound is typically synthesized through various chemical routes, and its properties, such as solubility and reactivity, make it a valuable component in the development of new chemical entities.

15561-50-9

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15561-50-9 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

Check Digit Verification of cas no

The CAS Registry Mumber 15561-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,6 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15561-50:
(7*1)+(6*5)+(5*5)+(4*6)+(3*1)+(2*5)+(1*0)=99
99 % 10 = 9
So 15561-50-9 is a valid CAS Registry Number.

15561-50-9Relevant academic research and scientific papers

Isoindolone derivatives, their preparation and the pharmaceutical compositions containing them

-

, (2008/06/13)

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

Convenient Preparation of Arylacetic Acids by Tetracarbonylcobaltate Anion Catalysed Carbonylation

Rao, B. Nageswara,Adapa, Srinivas R.,Pardhasaradhi, M.

, p. 84 - 85 (2007/10/02)

Tetracarbonylcobaltate catalyst -, has been prepared in 6 hr by pressure carbonylation of cobalt salt in aq alkaline solution containing cyanide catalyst.Carbonylation of arylchloromethyl derivatives in aq methanolic solutions using this catalyst affords arylacetic acids in good yields.

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