134510-06-8 Usage
Uses
Used in Pharmaceutical Industry:
5-Methoxy-2(1H)-pyrazinone is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its role in the creation of these compounds is crucial due to its unique chemical properties that can be leveraged to develop new medications and agricultural products.
Used in Flavor Industry:
5-Methoxy-2(1H)-pyrazinone is used as a flavoring agent for its distinctive odor and taste. Its ability to impart specific flavor profiles makes it a valuable ingredient in the development of food and beverage products, enhancing the sensory experience for consumers.
Used in Food Industry:
As a flavoring agent, 5-Methoxy-2(1H)-pyrazinone is used in the food industry to add unique taste and aroma characteristics to a variety of products. Its approval for use in food applications is a testament to its safety and the contribution it makes to the overall flavor profile of food items.
Used in Agrochemical Industry:
5-Methoxy-2(1H)-pyrazinone is also utilized in the agrochemical industry, where it serves as a building block for the synthesis of various agrochemicals. Its application in this field highlights its versatility and the potential for its use in developing new products that can benefit agricultural practices.
Check Digit Verification of cas no
The CAS Registry Mumber 134510-06-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,1 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134510-06:
(8*1)+(7*3)+(6*4)+(5*5)+(4*1)+(3*0)+(2*0)+(1*6)=88
88 % 10 = 8
So 134510-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2/c1-9-5-3-6-4(8)2-7-5/h2-3H,1H3,(H,6,8)
134510-06-8Relevant academic research and scientific papers
Studies on pyrazines, Part 39.1 Synthesis and acidic hydrolysis of 2-hydroxy-5-methoxypyrazine
Sato, Nobuhiro,Mizuno, Akio
, p. 747 - 749 (2007/10/03)
2-Hydroxy-5-methoxypyrazine was synthesised in a three-step reaction sequence starting from aminopyrazine. The product was extensively destroyed on acidic workup without forming 2,5-dihydroxypyrazine.
1, 3-dipolar cycloaddition reactions of benzonitrile oxide to 2(1II)-pyrazinone and its n- and o-methyl derivatives
Corsaro, Antonino,Chiacchio, Ugo,Pistara, Venerando,Perrini, Giancarlo
, p. 69 - 80 (2007/10/03)
2(1H)-Pyrazinone, which is in equilibrium with 2-pyrazinol, reacts with benzonitrile oxide (BNO) affording the N-adducl with a 67% yield, while 2-methoxypyrazine gives two methoxypyrazinones (ca. 3%) and a biscycloadduct together with its degradation product, which derive from the two unisolable monocycloadducts to the C=N4 double bond. Af-Methylpyrazinone gives only the degradation product (3.4%) of the initial monocycloadduct of BNO to C=N4: double bond.
