90316-38-4 Usage
Description
(2E)-3-(4-methoxyphenyl)-N,N-dimethylbut-2-enamide is an organic chemical compound belonging to the amide class, characterized by its but-2-enamide functional group and a 4-methoxyphenyl group. With a molecular formula of C13H19NO2, this compound is utilized in pharmaceuticals and organic synthesis due to its versatile chemical properties.
Uses
Used in Pharmaceutical Industry:
(2E)-3-(4-methoxyphenyl)-N,N-dimethylbut-2-enamide is used as an intermediate in the synthesis of other organic compounds, particularly for the development of new drugs. Its unique structure and functional groups contribute to its potential in creating novel pharmaceutical agents.
Used in Organic Synthesis:
In the field of organic synthesis, (2E)-3-(4-methoxyphenyl)-N,N-dimethylbut-2-enamide serves as a key component in the creation of various complex organic molecules. Its reactivity and structural features make it a valuable building block for synthesizing a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 90316-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,1 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 90316-38:
(7*9)+(6*0)+(5*3)+(4*1)+(3*6)+(2*3)+(1*8)=114
114 % 10 = 4
So 90316-38-4 is a valid CAS Registry Number.
90316-38-4Relevant articles and documents
Nickel-catalyzed cross-coupling of β-carbonyl alkenyl pivalates with arylzinc chlorides
Pan, Wen-Jing,Wang, Zhong-Xia
, p. 1029 - 1036 (2018/02/19)
The nickel-catalyzed cross-coupling reaction of β-carbonyl alkenyl pivalates with arylzinc reagents generates 3-aryl-substituted α,β-unsaturated carbonyl compounds via C-O bond cleavage. The reaction features mild reaction conditions, a wide scope of substrates, and good functional group tolerance.
