37398-49-5 Usage
Uses
Used in Pharmaceutical Industry:
2-ACETYL-ISONICOTINONITRILE is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving existing ones due to its unique chemical structure and reactivity.
Used in Agrochemical Industry:
In the agrochemical sector, 2-ACETYL-ISONICOTINONITRILE serves as an essential building block in the creation of pesticides and other agricultural chemicals, enhancing crop protection and yield.
Used in Dye Industry:
2-ACETYL-ISONICOTINONITRILE is utilized in the production of dyes, where its chemical properties allow for the development of novel colorants with specific characteristics for various applications.
Used in Material Science:
2-ACETYL-ISONICOTINONITRILE plays a role in the development of new materials, leveraging its reactivity to form compounds with unique properties for use in different industries, including electronics and textiles.
Used in Medicinal Chemistry Research:
As a key building block in medicinal chemistry, 2-ACETYL-ISONICOTINONITRILE is instrumental in the research and development of new therapeutic agents, facilitating advancements in drug discovery and design.
Check Digit Verification of cas no
The CAS Registry Mumber 37398-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,3,9 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37398-49:
(7*3)+(6*7)+(5*3)+(4*9)+(3*8)+(2*4)+(1*9)=155
155 % 10 = 5
So 37398-49-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O/c1-6(11)8-4-7(5-9)2-3-10-8/h2-4H,1H3
37398-49-5Relevant academic research and scientific papers
Rao, C. Janakiram,Agosta, William C.
, p. 2125 - 2131 (1994)
Stern-Volmer quenching of the photochemistry of 1c indicates that N- and O-abstraction (eqs 1 and 2, respectively) are quenched at different rates (Figure 1).For quenching of 2c kqτ is 157 M-1 and for 3c, 64 M-1.When 1c is sensitized with triplet sensitizers of increasing ET,N-abstraction increases (Table 1).These data indicate that N- and O-abstraction in 1c take place from distiguishable triplet states.Survey of Φp's of ring-substituted ketones 1b-d, 6d, 7a,b,d, 8b, 9b,d, 10b, and 11d demonstartes the effect of substitution on the competition between N- and O-abstraction (Table 2).For methyl- and dicyano-substituted ketones, the results can be understood simply in terms of shifts in ET of the n?* and ??* states of the heterocycle.The photochemistry of all these ketones requires consideration of interactions among three triplet states.
