17441-67-7 Usage
Uses
Used in Organic Synthesis:
[8-(hydroxymethyl)-7-bicyclo[2.2.2]oct-2-enyl]methanol is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows for a wide range of reactions, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [8-(hydroxymethyl)-7-bicyclo[2.2.2]oct-2-enyl]methanol is used as a building block for the development of new drugs. Its unique structure and reactivity may contribute to the creation of novel therapeutic agents with potential applications in treating various diseases.
Used in Agrochemical Industry:
[8-(hydroxymethyl)-7-bicyclo[2.2.2]oct-2-enyl]methanol may also find applications in the agrochemical industry, where it could be used as a starting material for the synthesis of new pesticides or other agrochemical products. Its unique properties could potentially lead to the development of more effective and environmentally friendly solutions for agricultural challenges.
Further Research:
Despite its potential applications, further research is necessary to fully understand the properties and potential uses of [8-(hydroxymethyl)-7-bicyclo[2.2.2]oct-2-enyl]methanol. This will help to unlock its full potential and contribute to the advancement of various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17441-67-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,4,4 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17441-67:
(7*1)+(6*7)+(5*4)+(4*4)+(3*1)+(2*6)+(1*7)=107
107 % 10 = 7
So 17441-67-7 is a valid CAS Registry Number.
17441-67-7Relevant academic research and scientific papers
Deuterium Kinetic Isotope Effects in the 1,4-Dimethylenecyclohexane Boat Cope Rearrangement
Gajewski, Joseph J.,Jimenez, Jose Leonardo
, p. 468 - 474 (2007/10/02)
In order to examine the extent of bond making in the boat-like 3,3-sigmatropic shift transition states, trans-2,3-dimethyl-1,4-dimethylenecyclohexane (T) and its exomethylene tetradeuteria derivative (TXD) were prepared.The 3,3-shift of TXD at 305 deg C r
