5106-58-1 Usage
Description
2-METHYL-2-PYRAZIN-2-YL-PROPIONITRILE, also known as MPN, is a chemical compound characterized by its molecular formula C8H8N2. It is a yellow liquid with a pungent odor and a high reactivity, making it a valuable reagent in organic synthesis. MPN is particularly utilized in the production of pharmaceuticals and agrochemicals, and also serves as an intermediate in the synthesis of dyes, pigments, and flavors. Due to its strong odor and reactivity, it is crucial to handle MPN with appropriate safety measures.
Uses
Used in Pharmaceutical Industry:
2-METHYL-2-PYRAZIN-2-YL-PROPIONITRILE is used as a reagent in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines. Its high reactivity allows for the creation of complex organic compounds that are essential in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2-METHYL-2-PYRAZIN-2-YL-PROPIONITRILE is employed as a reagent for the production of agrochemicals, which are vital for enhancing crop protection and yield.
Used in Dye and Pigment Synthesis:
2-METHYL-2-PYRAZIN-2-YL-PROPIONITRILE is used as an intermediate in the synthesis of dyes and pigments, playing a crucial role in the coloration of various materials and products.
Used in Flavor Production:
MPN is also utilized in the production of flavors, where its chemical properties contribute to the creation of unique taste profiles for food and beverage industries.
Check Digit Verification of cas no
The CAS Registry Mumber 5106-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5106-58:
(6*5)+(5*1)+(4*0)+(3*6)+(2*5)+(1*8)=71
71 % 10 = 1
So 5106-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3/c1-8(2,6-9)7-5-10-3-4-11-7/h3-5H,1-2H3
5106-58-1Relevant articles and documents
Mild and practical method for the α-arylation of nitriles with heteroaryl halides
Klapars, Artis,Waldman, Jacob H.,Campos, Kevin R.,Jensen, Mark S.,McLaughlin, Mark,Chung, John Y. L.,Cvetovich, Raymond J.,Chen, Cheng-Yi
, p. 10186 - 10189 (2007/10/03)
A mild and transition-metal-free method for theα-arylation of a liphatic nitriles with activated heteroaryl halides was developed using NaHMDS o r KHMDS as base at ambient temperature. The key to the success of this method is generation of the nitrile anion in the presence of the heteroaryl halide. The method is applicable to both primary and secondary carbonitriles and a wide range of heteroaryl halides. Selective monoarylation was observed with primary carbonitriles. The operational simplicity and the mild reaction conditions add to the value of this methodas a practical alternative to the preparation of α-heteroaryl carbonitriles.
