4925-61-5 Usage
Description
6-CHLORO-2-HYDROXYPYRAZINE is a chlorinated derivative of pyrazine with the molecular formula C4H4ClN3O, featuring a hydroxyl group. It is a colorless, crystalline solid with a slightly sweet odor and is widely used in various industries, including pharmaceutical, agricultural, and food and beverage, as a building block for the synthesis of drug molecules, agrochemicals, and as a flavoring agent. Its versatile nature and range of applications make it an important compound in the field of organic chemistry and chemical synthesis.
Uses
Used in Pharmaceutical Industry:
6-CHLORO-2-HYDROXYPYRAZINE is used as a building block for the synthesis of various drug molecules, contributing to the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agricultural Industry:
6-CHLORO-2-HYDROXYPYRAZINE is used as a building block for the synthesis of agrochemicals, such as pesticides and herbicides, to improve crop protection and yield.
Used in Food and Beverage Industry:
6-CHLORO-2-HYDROXYPYRAZINE is used as a flavoring agent to enhance the taste and aroma of various food and beverage products, providing a slightly sweet odor and contributing to the overall sensory experience.
Check Digit Verification of cas no
The CAS Registry Mumber 4925-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,2 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4925-61:
(6*4)+(5*9)+(4*2)+(3*5)+(2*6)+(1*1)=105
105 % 10 = 5
So 4925-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C4H3ClN2O/c5-3-1-6-2-4(8)7-3/h1-2H,(H,7,8)
4925-61-5Relevant articles and documents
Synthesis of Functionalized Pyrazin-2(1 H)-ones via Tele-Nucleophilic Substitution of Hydrogen Involving Grignard Reactants and Electrophiles
Mampuys, Pieter,Moseev, Timofey D.,Varaksin, Mikhail V.,De Houwer, Johan,Vande Velde, Christophe M. L.,Chupakhin, Oleg N.,Charushin, Valery N.,Maes, Bert U. W.
, p. 2699 - 2703 (2019)
The reaction of 6-chloro-1-methylpyrazin-2(1H)-one with Grignard reactants followed by quenching with different electrophiles gave access to a variety of 3,6-difunctionalized 1-methylpyrazin-2(1H)-ones. This regioselective three-component reaction represe
