97316-50-2 Usage
Uses
Used in Chemical Research:
Ethyl 4-cyano-2-pyridinecarboxylate is used as a reagent for various chemical reactions, contributing to advancements in the field of chemical research. Its stable structure and ability to participate in a range of reactions make it a valuable component in the synthesis of intermediate and final products.
Used in Pharmaceutical Research:
Ethyl 4-cyano-2-pyridinecarboxylate is used as a reagent in pharmaceutical research, aiding in the development of new drugs and compounds. Its chemical properties and reactivity are harnessed to produce potential therapeutic agents and contribute to the discovery of novel pharmaceuticals.
Used in Chemical Production:
Ethyl 4-cyano-2-pyridinecarboxylate is used in the production of various chemicals, where its reactivity and stability are essential for the synthesis of desired products. Its role in chemical production is crucial for the creation of a wide range of chemical substances used in different industries.
Safety Note:
Handling ethyl 4-cyano-2-pyridinecarboxylate requires due care, as it may be harmful if ingested, inhaled, or comes into contact with skin. Proper safety measures should be taken to minimize the risk of exposure and ensure the safe use of ethyl 4-cyano-2-pyridinecarboxylate in research and production settings.
Check Digit Verification of cas no
The CAS Registry Mumber 97316-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,3,1 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 97316-50:
(7*9)+(6*7)+(5*3)+(4*1)+(3*6)+(2*5)+(1*0)=152
152 % 10 = 2
So 97316-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2O2/c1-2-13-9(12)8-5-7(6-10)3-4-11-8/h3-5H,2H2,1H3
97316-50-2Relevant academic research and scientific papers
HOMOLYTIC ALKOXYCARBONYLATION REACTIONS IN TWO-PHASE SYSTEMS 3. INTRODUCTION OF A SINGLE CARBOXYLIC ACID ESTER FUNCTION INTO CYANO- OR ALKOXYCARBONYL SUBSTITUTED N-HETEROAROMATICS
Heinisch, Gottfried,Loetsch, Gerhard
, p. 731 - 744 (2007/10/02)
Homolytic alkoxycarbonylation reactions with cyanopyridines 1a, 2a, 3a, alkyl pyridinecarboxylates 1b, 2b, 3b, 3c and ethyl 4-pyridazinecarboxylate 4 in presence of dichloromethane were studied.It is demonstrated that under these conditions multiple substitution in general is suppressed markedly.Thus, this experimentally simple procedure represents an efficient and versatile method for single-step preparations of alkyl cyanopyridinecarboxylates 7a, 8a, 9a, 10a.Furthermore, it provides convenient access to so far not available mixed esters 5b, 7b, 8b, 10b, 13, derived from 2,3-pyridine-, 2,4-pyridine-, 3,4-pyridine and 4,5-pyridazinedicarboxylic acid.
