3469-07-6 Usage
Uses
Used in Organic Synthesis:
5-Methoxy-1H-indene is used as a building block in organic synthesis for its ability to introduce the indene moiety into organic molecules, facilitating the creation of a wide range of chemical compounds.
Used in Pharmaceutical Industry:
5-Methoxy-1H-indene is used as an intermediate in the synthesis of pharmaceuticals due to its unique structural properties, contributing to the development of new drugs with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Methoxy-1H-indene is utilized as a precursor in the production of agrochemicals, potentially enhancing crop protection and yield.
Used in Fragrance and Flavoring Industry:
5-Methoxy-1H-indene is used as a component in the production of fragrances and flavoring compounds, capitalizing on its aromatic characteristics to create desirable scents and tastes in various products.
Used in Medical Research:
5-Methoxy-1H-indene is studied for its potential medical applications, particularly in the treatment of neurological disorders, indicating its possible role in future therapeutic interventions.
Used as a Reagent in Chemical Reactions:
5-Methoxy-1H-indene serves as a reagent in chemical reactions, enabling the introduction of the indene structure into a variety of organic molecules for diverse applications across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 3469-07-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3469-07:
(6*3)+(5*4)+(4*6)+(3*9)+(2*0)+(1*7)=96
96 % 10 = 6
So 3469-07-6 is a valid CAS Registry Number.
3469-07-6Relevant articles and documents
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.
