22192-84-3 Usage
Uses
Used in Pharmaceutical Industry:
N-CYANOMETHYL-4-METHOXY-BENZAMIDE is used as a building block for the synthesis of various pharmaceuticals due to its versatile chemical structure and functional groups, which can be further modified to create new drug candidates.
Used in Agrochemical Industry:
In the agrochemical sector, N-CYANOMETHYL-4-METHOXY-BENZAMIDE is utilized as a starting material for the development of new agrochemicals, leveraging its chemical properties to create compounds with potential applications in crop protection and other agricultural areas.
Used in Organic Synthesis:
N-CYANOMETHYL-4-METHOXY-BENZAMIDE is employed as an intermediate in organic synthesis, where its functional groups can be manipulated to produce a range of organic compounds for various applications, including specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 22192-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,9 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22192-84:
(7*2)+(6*2)+(5*1)+(4*9)+(3*2)+(2*8)+(1*4)=93
93 % 10 = 3
So 22192-84-3 is a valid CAS Registry Number.
22192-84-3Relevant academic research and scientific papers
Synthesis of Imidazoles and Oxazoles via a Palladium-Catalyzed Decarboxylative Addition/Cyclization Reaction Sequence of Aromatic Carboxylic Acids with Functionalized Aliphatic Nitriles
Dai, Ling,Yu, Shuling,Lv, Ningning,Ye, Xuanzeng,Shao, Yinlin,Chen, Zhongyan,Chen, Jiuxi
supporting information, p. 5664 - 5668 (2021/08/01)
We herein report an efficient approach for the assembly of multiply substituted imidazoles and oxazoles in a single-step manner. These transformations are based on a decarboxylation addition and annulation of readily accessible aromatic carboxylic acids a
Aminolysis of Benzoyl Fluorides in Water
Song, Byeong Doo,Jencks, William P.
, p. 8479 - 8484 (2007/10/02)
The reactions of benzoyl fluorides (p-Me2N, p-MeO, m-Cl) with primary amines of pKa = 3.9-11 in aqueous solution follow a first-order dependence on amine concentration and the addition of 0.83 M potassium phosphate, 10percent dianion, does not
