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α-(2-methoxyphenyl)-α-(methylthio)acetonitrile is an organic compound with the chemical formula C10H11NO2S. It is a derivative of acetonitrile, featuring a 2-methoxyphenyl group and a methylthio group attached to the alpha carbon. α-(2-methoxyphenyl)-α-(methylthio)acetonitrile is characterized by its aromatic ring with a methoxy substituent at the 2nd position and a methylthio group at the alpha carbon, which is also bonded to a nitrile group. It is a colorless liquid with a molecular weight of 213.26 g/mol. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of pesticides and other chemical compounds. Due to its reactivity and potential applications, it is an important compound in the field of organic chemistry.

84784-26-9

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84784-26-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84784-26-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,8 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 84784-26:
(7*8)+(6*4)+(5*7)+(4*8)+(3*4)+(2*2)+(1*6)=169
169 % 10 = 9
So 84784-26-9 is a valid CAS Registry Number.

84784-26-9Downstream Products

84784-26-9Relevant academic research and scientific papers

Syntheses of Arylacetone and Arylacetonitrile by Friedel-Crafts Reaction with α-Chloro-α-(methylthio)-substituted Acetone and Acetonitrile

Tamura, Yasumitsu,Choi, Hong Dae,Mizutani, Masako,Ueda, Yuko,Ishibashi, Hiroyuki

, p. 3574 - 3579 (2007/10/02)

Novel preparative methods for arylacetone and arylacetonitrile are described.Friedel-Crafts reactions of aromatic compounds with α-chloro-α-(methylthio)acetone (4) and α-chloro-α-(methylthio)acetonitrile (7) in the presence of Lewis acid afforded α-(methylthio)arylacetone (5) and α-(methylthio)arylacetonitrile (8), respectively.Compounds (5) and (8) were converted into the corresponding arylacetone (6) and arylacetonitrile (9) by reduction with zinc dust in acetic acid.Keywords: Friedel-Crafts reaction with α-chloro-α-(methylthio)acetone; Friedel-Crafts reaction with α-chloro-α-(methylthio)acetonitrile; α-(methylthio)arylacetone; α-(methylthio)arylacetonitrile; arylacetone; arylacetonitrile; reductive desulfurization; zinc dust-acetic acid

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