10319-80-9 Usage
Uses
Used in Analytical Chemistry:
N-(1-naphthyl)thioacetamide is used as a reagent for the detection and determination of various metal cations due to its ability to form stable complexes with metal ions.
Used in Organic Synthesis:
N-(1-naphthyl)thioacetamide is used as an intermediate in the synthesis of various organic compounds, contributing to the development of new chemical entities.
Used in Pharmaceutical and Agrochemical Industries:
N-(1-naphthyl)thioacetamide is used as a starting material or building block in the synthesis of pharmaceuticals and agrochemicals, potentially leading to the discovery of new drugs and pesticides.
Used in Corrosion Inhibition:
N-(1-naphthyl)thioacetamide has been studied for its potential as a corrosion inhibitor, offering a possible solution for protecting materials from degradation in various industrial applications.
Used in Biological Imaging:
N-(1-naphthyl)thioacetamide has been explored as a fluorescent dye in biological imaging, which could enhance the visualization of cellular and molecular processes in research and diagnostics.
It is crucial to handle N-(1-naphthyl)thioacetamide with care, as it is considered a hazardous chemical. Proper ventilation and personal protective equipment are necessary when working with N-(1-naphthyl)thioacetamide to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 10319-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,1 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10319-80:
(7*1)+(6*0)+(5*3)+(4*1)+(3*9)+(2*8)+(1*0)=69
69 % 10 = 9
So 10319-80-9 is a valid CAS Registry Number.
10319-80-9Relevant academic research and scientific papers
Facile synthesis of thioamides via P2S5-mediated beckmann rearrangement of oximes
Li, Jiangsheng,Cheng, Chao,Zhang, Xinrui,Li, Zhiwei,Cai, Feifei,Xue, Yuan,Liu, Weidong
, p. 1687 - 1689 (2012/10/29)
A facile and efficient approach to the synthesis of secondary thioamides from ketoximes via Beckmann rearrangement has been established, using phosphorus pentasulfide as a dehydrating and thiating agent. It is also efficient for the preparation of primary thiobenzamide from benzaldoxime. This approach features simple-operation, easy-control and good to excellent yields.