58265-35-3 Usage
Uses
Used in Pharmaceutical Industry:
2,2,3-trimethyl-N-phenyl-butanamide is utilized as an intermediate in the synthesis of various pharmaceuticals due to its unique chemical structure and pharmacological properties. Its antinociceptive and anti-inflammatory effects make it a valuable component in the development of medications aimed at treating pain and inflammation.
Used in Agrochemical Industry:
In the agrochemical sector, 2,2,3-trimethyl-N-phenyl-butanamide serves as an intermediate in the production of agrochemicals, contributing to the development of compounds with specific pesticidal or herbicidal activities, thereby enhancing crop protection and yield.
Used in Organic Synthesis:
2,2,3-trimethyl-N-phenyl-butanamide is employed as a building block in organic synthesis, allowing for the creation of new compounds with improved or novel properties. Its versatile structure facilitates its use in the synthesis of a wide range of organic compounds for various applications.
Used in Research and Development:
2,2,3-trimethyl-N-phenyl-butanamide is also used in research and development settings for studying its pharmacological activities and exploring its potential applications in medicine and other fields. The ongoing research on 2,2,3-trimethyl-N-phenyl-butanamide aims to uncover new uses and optimize its properties for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 58265-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,2,6 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58265-35:
(7*5)+(6*8)+(5*2)+(4*6)+(3*5)+(2*3)+(1*5)=143
143 % 10 = 3
So 58265-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H19NO/c1-10(2)13(3,4)12(15)14-11-8-6-5-7-9-11/h5-10H,1-4H3,(H,14,15)
58265-35-3Relevant academic research and scientific papers
Iron-Catalyzed Oxidative Coupling Reaction of Isocyanides and Simple Alkanes towards Amide Synthesis
Yuan, Hongdong,Liu, Zhiqiang,Shen, Yushu,Zhao, Hongbin,Li, Chunju,Jia, Xueshun,Li, Jian
supporting information, p. 2009 - 2013 (2019/03/21)
An iron-catalyzed oxidative coupling reaction of isocyanide and readily available alkane has been disclosed. In the presence of a catalytic amount of FeCp2 (10 mol%), heating a mixture of alkane, isocyanide, and DTBP in DCE allows for the formation of an amide. This reaction tolerates many simple alkanes including cycloalkanes and chain alkanes. Furthermore, a series of aromatic isocyanides having different substituents on the aromatic ring are also proven to be effective reaction components. Unfortunately, the employment of aliphatic isocyanides fails to afford the desired products. The present strategy avoids tedious procedures and the employment of toxic starting materials, thus providing an environmentally benign and efficient protocol towards amide synthesis. (Figure presented.).
