1216-01-9 Usage
Uses
Used in Organic Synthesis:
Pyridinium, 4-(methoxycarbonyl)-1-(phenylmethyl)-, iodide is used as a reagent for various transformations in organic synthesis. Its ability to participate in a range of reactions makes it a valuable component in the synthesis of complex organic molecules.
Used as a Catalyst in Chemical Reactions:
Pyridinium, 4-(methoxycarbonyl)-1-(phenylmethyl)-, iodide is employed as a catalyst in reactions such as the formation of esters, amides, and other organic functional groups. Its unique structure allows it to facilitate these reactions, enhancing the efficiency and selectivity of the process.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Pyridinium, 4-(methoxycarbonyl)-1-(phenylmethyl)-, iodide is used as a catalyst for the synthesis of various drug molecules. Its ability to participate in key reactions helps in the development of new and improved pharmaceutical compounds.
Used in Material Science:
Pyridinium, 4-(methoxycarbonyl)-1-(phenylmethyl)-, iodide is also used in material science for the synthesis of advanced materials with specific properties. Its versatility in participating in various chemical reactions allows for the creation of materials with tailored characteristics for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1216-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1216-01:
(6*1)+(5*2)+(4*1)+(3*6)+(2*0)+(1*1)=39
39 % 10 = 9
So 1216-01-9 is a valid CAS Registry Number.
1216-01-9Relevant academic research and scientific papers
Feliz, Miguel,Bosch, Joan,Mauleon, David,Amat, Mercedes,Domingo, Antonio
, p. 2435 - 2440 (1982)
2-Cyano-1,2,3,6-tetrahydropyridines 2b-d, with a functionalized C-4 substituent, were prepared from the corresponding pyridinium salts by sodium borohydride reduction in the presence of sodium cyanide.Reaction of these 2-cyanotetrahydropyridines with indolylmagnesium iodide afforded 3-(1,2,3,6-tetrrahydro-2-pyridyl)indoles 3b-d.Alternatively, 3c and 3d were prepared in excellent yield by condensation of 2-cyanotetrahydropyridines 2c and 2d with indole in acetic acid medium.Deethyldasycarpidone was obtained from 3b in poor or moderate yields by three alternative procedures and from 3c in a three-step sequence.The preparation of deethyldasycarpidone from 2-cyanotetrahydropyridine 2c via the (tetrahydropyridyl)indole 3c constitutes an improved synthesis of this tetracyclic ring system.Similarly, 20-deethyl-4-demethyldasycarpidone was obtained from (tetrahydropyridyl)indole 3d.
