914360-88-6 Usage
Uses
Used in Pharmaceutical Industry:
3-chloro-2-pyrazineacetonitrile is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique reactivity allows for the creation of a wide range of drug molecules, contributing to the development of new treatments and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 3-chloro-2-pyrazineacetonitrile is employed as an intermediate for the production of agrochemicals. Its role in the synthesis of various agrochemicals aids in the development of effective solutions for pest control and crop protection.
Used in Medicinal Chemistry:
3-chloro-2-pyrazineacetonitrile is utilized as a building block in the synthesis of pyrazine-based heterocycles, which are significant in medicinal chemistry. These heterocycles are integral to the development of novel drug candidates with potential therapeutic applications.
Used in Materials Science:
In the field of materials science, 3-chloro-2-pyrazineacetonitrile is used in the synthesis of pyrazine-based heterocycles that have potential applications in the development of new materials with unique properties, such as conductivity, magnetism, or optical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 914360-88-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,3,6 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 914360-88:
(8*9)+(7*1)+(6*4)+(5*3)+(4*6)+(3*0)+(2*8)+(1*8)=166
166 % 10 = 6
So 914360-88-6 is a valid CAS Registry Number.
914360-88-6Relevant articles and documents
Highly selective substitutions in 2,3-dichloropyrazine. A novel general approach to aloisines
Chekmarev, Dmitriy S.,Shorshnev, Sergey V.,Stepanov, Alexander E.,Kasatkin, Alexander N.
, p. 9919 - 9930 (2006)
A highly efficient synthesis of the potent CDKs (cyclin-dependent kinases) inhibitors, aloisines (substituted 5H-pyrrolo[2,3-b]pyrazines) is presented. The method is based on highly selective monosubstitution of a single chlorine atom in 2,3-dichloropyraz
