78495-64-4 Usage
Description
(2-fluoro-3,4-dimethoxyphenyl)acetonitrile, also known as FDMA, is a chemical compound with the molecular formula C10H10FNO2. It is a nitrile derivative of 2-fluoro-3,4-dimethoxyacetophenone, characterized by its unique chemical structure and properties. FDMA is commonly used as a building block in the synthesis of pharmaceuticals and agrochemicals, and has been found to exhibit significant anti-inflammatory and analgesic properties.
Uses
Used in Pharmaceutical Industry:
(2-fluoro-3,4-dimethoxyphenyl)acetonitrile is used as a building block for the synthesis of pharmaceuticals due to its unique chemical structure and properties. Its significant anti-inflammatory and analgesic properties make it a valuable component in the development of potential new drug candidates.
Used in Agrochemical Industry:
(2-fluoro-3,4-dimethoxyphenyl)acetonitrile is used as a building block for the synthesis of agrochemicals, contributing to the development of effective and innovative products in this field.
Used in Organic Chemistry:
(2-fluoro-3,4-dimethoxyphenyl)acetonitrile is used as a valuable tool for researchers and scientists in organic chemistry due to its diverse reactivity and functional groups.
Used in Material Science:
(2-fluoro-3,4-dimethoxyphenyl)acetonitrile has potential applications in material science, where its unique chemical structure and properties can be utilized for the development of new materials and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 78495-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,9 and 5 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78495-64:
(7*7)+(6*8)+(5*4)+(4*9)+(3*5)+(2*6)+(1*4)=184
184 % 10 = 4
So 78495-64-4 is a valid CAS Registry Number.
78495-64-4Relevant articles and documents
Catechol derivatives
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, (2008/06/13)
Catechol derivatives of the formula STR1 wherein Ra, Rb and Rc have the significance given herein, the ester and ether derivatives thereof which are hydrolyzable under physiological conditions and the pharmaceutically acceptable salts thereof are described and possess valuable pharmacological properties. In particular, they inhibit the enzyme catechol-O-methyltransferase (COMT), a soluble, magnesium-dependent enzyme which catalyses the transference of the methyl group of S-adensoylmethionine to a catechol substrate, whereby the corresponding methyl ethers are formed. Suitable substrates which can be O-methylated by COMT and which can thus be deactivated are, for example, extraneuornal catecholamines and exogeneously-administered therapeutically active substances having a catechol structure. Formula Ia above embraces not only compounds which form part of the invention, but also known compounds; the compounds which form part of the invention can be prepared according to known methods.
