21864-76-6 Usage
Uses
Used in Chemical Synthesis:
2-Ethyl-2-methylbutyronitirle is used as a key intermediate in the synthesis of various chemicals, contributing to the production of agrochemicals, pharmaceuticals, and dyes. Its versatile chemical properties make it a valuable component in the creation of a wide range of products.
Used in Solvent Applications:
In the chemical industry, 2-Ethyl-2-methylbutyronitirle is utilized as a solvent in various chemical reactions. Its ability to dissolve a broad spectrum of substances enhances the efficiency and effectiveness of these processes.
Used in Pesticide Formulation:
2-Ethyl-2-methylbutyronitirle is employed as a stabilizer in the formulation of certain pesticides. Its inclusion helps to maintain the stability and performance of these products, ensuring their effectiveness in controlling pests.
Used in Pharmaceutical Industry:
2-Ethyl-2-methylbutyronitirle is used as a raw material in the synthesis of pharmaceuticals, playing a crucial role in the development of new drugs and medicines.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Ethyl-2-methylbutyronitirle is used as a starting material for the production of various agrochemicals, such as insecticides and herbicides, which are essential for protecting crops and ensuring food security.
Used in Dye Industry:
2-Ethyl-2-methylbutyronitirle is also utilized in the dye industry as a precursor for the synthesis of different types of dyes, contributing to the vibrant colors found in textiles, plastics, and other materials.
Check Digit Verification of cas no
The CAS Registry Mumber 21864-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,6 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21864-76:
(7*2)+(6*1)+(5*8)+(4*6)+(3*4)+(2*7)+(1*6)=116
116 % 10 = 6
So 21864-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H13N/c1-4-7(3,5-2)6-8/h4-5H2,1-3H3
21864-76-6Relevant academic research and scientific papers
Wanderungstendenzen cyclischer, polycyclischer und methylverzweigter Alkylreste bei der Beckmann-Umlagerung
Langhals, Heinz,Ruechardt, Christoph
, p. 3831 - 3854 (2007/10/02)
The migration aptitudes of polycyclic bridgehead groups, cycloalkyl groups as well as of β-, γ- and δ-branched alkyl groups in the Chapman variant of the Beckmann rearrangement were determined.From these data it is concluded that at transition state 2 the migrating group is not resembling a planarised carbenium ion R+, but rather a pentacoordinated carbonium ion structure.Because only small geometrical changes occur in the migrating group vertical stabilisation of charge at transition state is believed to have significant influence on the migration aptitudes.
