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2-(2,5-dimethylphenyl)-2-phenylacetonitrile is an organic compound with the molecular formula C18H17N. It is a derivative of acetonitrile, featuring a phenyl group attached to the acetonitrile moiety. The compound has a 2,5-dimethylphenyl group substituted at the 2-position, which consists of a benzene ring with two methyl groups at the 2nd and 5th positions. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides and other specialty chemicals. Its structure provides a unique combination of aromatic and aliphatic characteristics, which can influence its reactivity and physical properties in chemical reactions.

82954-08-3

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82954-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82954-08-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,5 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 82954-08:
(7*8)+(6*2)+(5*9)+(4*5)+(3*4)+(2*0)+(1*8)=153
153 % 10 = 3
So 82954-08-3 is a valid CAS Registry Number.

82954-08-3Downstream Products

82954-08-3Relevant academic research and scientific papers

Palladium-Catalyzed Direct α-Arylation of Arylacetonitriles with Aryl Tosylates and Mesylates

Yuen, On Ying,Chen, Xiangmeng,Wu, Junyu,So, Chau Ming

supporting information, p. 1912 - 1916 (2020/03/13)

The first general palladium-catalyzed α-arylation of arylacetonitriles with aryl and heteroaryl sulfonates are reported. Pd(OAc)2 associated with XPhos serves as the effective catalyst to facilitate this reaction. A broad range of electron-rich, -neutral, -deficient, and sterically hindered aryl/heteroaryl tosylates and mesylates are coupled with arylacetonitriles bearing different substituents to give the corresponding products in good to excellent yields. Catalyst loading down to 0.1 mol-% Pd was achieved, and 22 unprecedented compounds were synthesized from 43 demonstrated examples using this method. Its applicability with the modification of biological phenolic compounds was successfully demonstrated. The Pd/XPhos system catalyzed the α-arylation and followed by alkylation in one-pot sequential conditions, resulting in the direct synthesis of compounds containing quaternary center- and deuterium-containing compounds in good to excellent yields.

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