6784-62-9 Usage
Uses
Used in Food Industry:
1-Pyrazin-2-yl-propan-2-one is used as a flavoring agent for its nutty and roasted notes, enhancing the taste and aroma of various food products.
Used in Perfumery:
1-Pyrazin-2-yl-propan-2-one is used as a fragrance compound in perfumes, contributing to the creation of complex and appealing scents.
Used in Pharmaceutical Synthesis:
1-Pyrazin-2-yl-propan-2-one serves as a precursor in the production of pharmaceuticals, playing a crucial role in the synthesis of various medicinal compounds.
Used in Agrochemical Synthesis:
In the agrochemical industry, 1-Pyrazin-2-yl-propan-2-one is used as a precursor for the synthesis of agrochemicals, contributing to the development of effective products for agricultural applications.
Used in Organic Compound Production:
1-Pyrazin-2-yl-propan-2-one is utilized as a precursor in the production of various organic compounds, showcasing its versatility in chemical synthesis.
However, it is important to note that exposure to 1-pyrazin-2-yl-propan-2-one may cause irritation to the skin, eyes, and respiratory system. Therefore, it should be handled with care in a well-ventilated area to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 6784-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6784-62:
(6*6)+(5*7)+(4*8)+(3*4)+(2*6)+(1*2)=129
129 % 10 = 9
So 6784-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O/c1-6(10)4-7-5-8-2-3-9-7/h2-3,5H,4H2,1H3
6784-62-9Relevant academic research and scientific papers
Novel Compounds
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, (2008/06/13)
The invention relates to heteroaromatic carboxamides of formula (I), wherein A, R1, R2 and X are as defined in the specification, processes and intermediates used in their preparation, pharmaceutical compositions containing them and their use in therapy.
SRN1 Mechanism in Heteroaromatic Nucleophilic Substitution. Reactions Involving Halogenated Pyrimidines, Pyridazines, and Pyrazines
Carver, David R.,Komin, Andrew P.,Hubbard, James S.,Wolfe, James S.
, p. 294 - 299 (2007/10/02)
Reactions of 2-chloropyrimidine (1), 4-chloro-2,6-dimethoxypyrimidine (7), 3-chloro-6-methoxypyridazine (9), and 2-chloropyrazine (14) with a representative series of ketone enolates in liquid ammonia exhibited characteristics consistent with a radical-chain (SRN1) mechanism for substituton.Diazines 1 and 9 showed an unexpected sensitivity to enolate ion structure, with 1 reacting best with tertiary enolates and 9 undergoing substitution most satisfactorily with primary enolates.The order of SRN1 reactivity among the various substrates was found to be 14 > 9 > 7 =ca. 1.Thus 1 and 7 required photostimulation at 35o nm for satisfactory displacemement of chloride, 9 underwent some substitution without illumination, and 14 reacted smoothly in the dark.
