26947-41-1 Usage
Uses
Used in Analytical Chemistry:
3-Isoquinolinecarbonitrile is used as an analytical standard for studying the thermal degradation of 2-chlorobenzylidenemalononitrile (CS riot control agent) at elevated temperatures. Its role in this application is to provide a reference point for the analysis and comparison of the degradation process, ensuring accurate and reliable results.
Used in Pharmaceutical Research:
Although not explicitly mentioned in the provided materials, 3-Isoquinolinecarbonitrile, due to its structural properties, has the potential to be used in the development of pharmaceutical compounds. Its aromatic and nitrogen-containing structure can be exploited in the design of new drugs targeting various biological receptors, such as enzymes or ion channels.
Used in Chemical Synthesis:
3-Isoquinolinecarbonitrile can also be utilized as a starting material or intermediate in the synthesis of more complex organic compounds, particularly those with potential applications in the pharmaceutical, agrochemical, or materials science industries. Its reactivity and functional groups can be further modified to create a diverse range of products.
Synthesis Reference(s)
Canadian Journal of Chemistry, 32, p. 641, 1954 DOI: 10.1139/v54-084
Check Digit Verification of cas no
The CAS Registry Mumber 26947-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,4 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 26947-41:
(7*2)+(6*6)+(5*9)+(4*4)+(3*7)+(2*4)+(1*1)=141
141 % 10 = 1
So 26947-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H6N2/c11-6-10-5-8-3-1-2-4-9(8)7-12-10/h1-5,7H
26947-41-1Relevant academic research and scientific papers
A practical 'one-pot' synthesis of ethyl isoquinoline-3-carboxylate by domino reactions: A potential entry to constrained nonproteogenic amino acid derivatives
Ameur Meziane, Mohamed A?t,Royer, Sylvain,Bazureau, Jean Pierre
, p. 1017 - 1020 (2007/10/03)
Two simple and efficient 'one-pot' preparations of isoquinoline-3-carboxylates by domino reactions using phthalaldehydes and imidate (route A) or diethyl aminomalonate (route B) are described. The third route involves the use of ethyl glycinate, aminoacet
