2359-64-0 Usage
Uses
Used in Pharmaceutical Industry:
Cyclohexanepropanenitrile, 2-methyleneis used as a starting material for the synthesis of various pharmaceuticals. Its chemical structure allows for the creation of a wide range of drug molecules, making it a valuable component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical industry, Cyclohexanepropanenitrile, 2-methyleneis employed as a starting material for the production of agrochemicals. Its versatility in chemical reactions enables the synthesis of compounds that can be used in the development of pesticides, herbicides, and other agricultural products.
Used in Specialty Chemicals Production:
Cyclohexanepropanenitrile, 2-methyleneis used as a raw material in the production of specialty chemicals. Its unique properties make it suitable for the synthesis of compounds used in various industries, such as plastics, coatings, and adhesives.
Used as a Solvent in Chemical Processes:
Cyclohexanepropanenitrile, 2-methyleneis utilized as a solvent in various chemical processes. Its ability to dissolve a wide range of substances makes it a valuable asset in the chemical industry, facilitating reactions and improving the efficiency of production processes.
Used in Chemical Research and Development:
Cyclohexanepropanenitrile, 2-methyleneis employed as a research chemical in the development of new chemical compounds and processes. Its reactivity and compatibility with other chemicals make it an essential tool for scientists and researchers working in the field of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 2359-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2359-64:
(6*2)+(5*3)+(4*5)+(3*9)+(2*6)+(1*4)=90
90 % 10 = 0
So 2359-64-0 is a valid CAS Registry Number.
2359-64-0Relevant academic research and scientific papers
Palladium-Catalyzed Aerobic Oxidative Cyclization of Aliphatic Alkenyl Amides for the Construction of Pyrrolizidine and Indolizidine Derivatives
Lo, Kai-Yip,Ye, Liu,Yang, Dan
, p. 1570 - 1575 (2017/08/11)
An efficient palladium-catalyzed aerobic oxidative cyclization has been developed to synthesize a variety of pyrrolizidine and indolizidine derivatives from simple aliphatic alkenyl amides in moderate to good yields. The reaction features the capability of accessing various N-heterocycles and the use of molecular oxygen (1 atm) as the green oxidant.
Diastereoselectivity control of the radical carboazidation of substituted methylenecyclohexanes
Cren, Sylvaine,Schar, Pascal,Renaud, Philippe,Schenk, Kurt
supporting information; experimental part, p. 2942 - 2946 (2009/09/06)
A systematic study of the diastereoselectivity of the radical carboazidation of methylenecyclohexane derivatives is presented. Several substitution patterns leading to a high level of stereocontrol have been identified. Axial attack is the preferred reaction pathway for cyclohexyl radicals, and excellent stereoselectivities can be obtained by introducing an axial substitutent at position 2. In this case, a second equatorial substituent at position 2 may be tolerated without a large detrimental effect on the diastereoselectivity. Finally, a high level of equatorial attack is observed with a very bulky substituent at position 2.
