103698-09-5 Usage
Uses
Used in Pharmaceutical Industry:
4-Pyridinecarbonitrile,3-nitro-(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure and reactivity make it a valuable component in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Pyridinecarbonitrile,3-nitro-(9CI) serves as a crucial building block for the creation of novel pesticides. Its properties contribute to the formulation of effective and innovative agrochemical products.
Used in Organic Synthesis:
4-Pyridinecarbonitrile,3-nitro-(9CI) is utilized as a versatile building block in organic synthesis, enabling the production of a wide range of organic compounds for various applications.
It is important to handle 4-Pyridinecarbonitrile,3-nitro-(9CI) with care due to potential health and environmental risks if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 103698-09-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,9 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103698-09:
(8*1)+(7*0)+(6*3)+(5*6)+(4*9)+(3*8)+(2*0)+(1*9)=125
125 % 10 = 5
So 103698-09-5 is a valid CAS Registry Number.
103698-09-5Relevant articles and documents
The synthesis of β-nitropyridine compounds
Bakke, Jan M.,Ranes, Eli,Riha, Jaroslav,Svensen, Harald
, p. 141 - 144 (2007/10/03)
Pyridine and a number of substituted pyridines have been nitrated by reaction with N2O5 followed by reaction with an aqueous solution of SO2xH2O or NaHSO3. The dependence of the yields on the pH of the aqueous reaction medium, on the concentration of SO2xH2O-HSO3-, on addition of methanol to the aqueous phase, and on the reaction temperature were investigated. The yields obtained with NaHSO3 were: 3-nitropyridine 77%, 2-methyl-5-nitro-pyridine 36%, 3-methyl-5-nitropyridinc 24%, 3-acetyl-5-nitropyridine 18%, 5-nitropyridine-3-carboxylic acid 15%, 3-chloro-5-nitropyridine 11%, 4-methyl-3-nitropyridine 39%, 4-acetyl-3-nitropyridine 67%, 4-cyano-3-nitropyridine 45%, 4-phenyl-3-nitropyridine 68%, 4-formyl-3-nitropyridine 62% (from reaction in liquid SO2), 3-nitropyridine-4-carboxylic acid 48%, methyl 3-nitropyridine-4-carboxylate 75%, 2,3-dimethyl-5-nitropyridine 37%, 2,4-dimethyl-5-nitropyridine 64%, 3-nitroquinoline 10% and 4-nitroisoquinoline 42%.
