103582-50-9 Usage
Uses
Used in Organic Synthesis:
3-(1-methoxyethenyl)tricyclo[2.2.1.0~2,6~]heptane is used as a valuable intermediate for the production of various pharmaceutical and agrochemical compounds. Its unique structure and reactivity make it a key component in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(1-methoxyethenyl)tricyclo[2.2.1.0~2,6~]heptane is used as a building block for the development of new drugs. Its conformational constraints and enhanced stereochemical control contribute to the creation of more efficient synthetic routes for drug production.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 3-(1-methoxyethenyl)tricyclo[2.2.1.0~2,6~]heptane is utilized as a key intermediate for the synthesis of various agrochemical compounds, such as pesticides and herbicides, due to its unique structural properties and reactivity.
Used in Chemical Research:
3-(1-methoxyethenyl)tricyclo[2.2.1.0~2,6~]heptane is also used in chemical research as a model compound for studying the effects of conformational constraints on chemical reactions and the development of novel synthetic methodologies. Its extensive study has contributed to the advancement of organic chemistry and the discovery of new synthetic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 103582-50-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,5,8 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103582-50:
(8*1)+(7*0)+(6*3)+(5*5)+(4*8)+(3*2)+(2*5)+(1*0)=99
99 % 10 = 9
So 103582-50-9 is a valid CAS Registry Number.
103582-50-9Relevant academic research and scientific papers
Thermodynamics of Vinyl Ethers. XXX. On the Ease of Introduction of a C=C bond Exocyclic to Some Bi- and Tricyclic Rings
Taskinen, Esko
, p. 779 - 784 (2007/10/02)
The ease of introduction of a C=C bond exocyclic to a norbornane, norbornene and nortricyclane ring has been studied by chemical equilibration of the isomeric methyl enol ethers of 2-acetylnorbornane, 2-acetylnorbornene and 3-acetylnortricyclane.The process in question is seen to become increasingly more difficult in the sequence norbornane-1 less favored, and that to a nortricyclane ring ca. 13 kJ mol-1 less favored than the introduction of a C=C bond exocyclic to a norbornane ring.Thermodynamic data for other isomerization reactions are also given.
