20762-98-5 Usage
Uses
Used in Organic Synthesis:
2-FUROYL AZIDE is used as a reagent in organic synthesis for the preparation of various compounds. Its unique molecular structure allows it to participate in a range of chemical reactions, making it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Development:
2-FUROYL AZIDE is used as a starting material in the development of new pharmaceuticals. Its potential applications in this field are currently being explored, with the aim of discovering novel drug candidates that can address unmet medical needs.
Used in Agrochemical Development:
2-FUROYL AZIDE is also used in the development of new agrochemicals. Its potential as a building block for the creation of innovative and effective crop protection products is being investigated, with the goal of enhancing agricultural productivity and sustainability.
Used in Research and Development:
2-FUROYL AZIDE is utilized in research and development settings to study its properties and explore its potential applications in various fields. This includes the investigation of its reactivity, stability, and compatibility with other chemicals, as well as its potential use in the synthesis of new materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 20762-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,6 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20762-98:
(7*2)+(6*0)+(5*7)+(4*6)+(3*2)+(2*9)+(1*8)=105
105 % 10 = 5
So 20762-98-5 is a valid CAS Registry Number.
20762-98-5Relevant academic research and scientific papers
Yu, Tian-Yang,Zheng, Zhao-Jing,Dang, Tong-Tong,Zhang, Fang-Xia,Wei, Hao
, p. 10589 - 10594 (2018)
A metal-free PhI(OAc)2-mediated method for the synthesis of acyl azides through oxidative cleavage of 1,3-diketones is described. This method is shown to have a broad substrate scope, providing a useful tool for multiproduct synthesis in a single procedure. A possible reaction pathway is proposed based on mechanistic studies.
