113075-75-5 Usage
Uses
Used in Chemical Industry:
8-CHLORO-1,2-DIHYDRO-NAPHTHALENE is used as a key intermediate in the synthesis of various industrial products due to its chemical properties, facilitating the creation of dyes, pesticides, and pharmaceuticals.
Used in Dye Production:
In the dye industry, 8-CHLORO-1,2-DIHYDRO-NAPHTHALENE is used as a precursor for the development of specific dyes, contributing to the coloration and performance of these products.
Used in Pesticide Formulation:
8-CHLORO-1,2-DIHYDRO-NAPHTHALENE is utilized as a component in the formulation of certain pesticides, enhancing their effectiveness in controlling pests and contributing to agricultural productivity.
Used in Pharmaceutical Development:
In the pharmaceutical sector, 8-CHLORO-1,2-DIHYDRO-NAPHTHALENE is employed as a building block for the synthesis of various medicinal compounds, playing a crucial role in drug discovery and development processes.
Check Digit Verification of cas no
The CAS Registry Mumber 113075-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,7 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113075-75:
(8*1)+(7*1)+(6*3)+(5*0)+(4*7)+(3*5)+(2*7)+(1*5)=95
95 % 10 = 5
So 113075-75-5 is a valid CAS Registry Number.
113075-75-5Relevant academic research and scientific papers
AuCl3-Catalyzed Ring-Closing Carbonyl–Olefin Metathesis
Wang, Rui,Chen, Yi,Shu, Mao,Zhao, Wenwen,Tao, Maoling,Du, Chao,Fu, Xiaoya,Li, Ao,Lin, Zhihua
supporting information, p. 1941 - 1946 (2020/02/11)
Compared with the ripeness of olefin metathesis, exploration of the construction of carbon–carbon double bonds through the catalytic carbonyl–olefin metathesis reaction remains stagnant and has received scant attention. Herein, a highly efficient AuCl3-catalyzed intramolecular ring-closing carbonyl–olefin metathesis reaction is described. This method features easily accessible starting materials, simple operation, good functional-group tolerance and short reaction times, and provides the target cyclopentenes, polycycles, benzocarbocycles, and N-heterocycle derivatives in good to excellent yields.
