908279-57-2 Usage
Uses
Used in Pharmaceutical and Agrochemical Industries:
3-IODO-2-METHOXYISONICOTINONITRILE is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its strong electron-withdrawing properties, which facilitate various chemical reactions essential in the production of these compounds.
Used in Organic Synthesis:
3-IODO-2-METHOXYISONICOTINONITRILE is used as a building block in organic synthesis for the creation of heterocyclic compounds. Its unique structure and functional groups make it a valuable component in the development of complex organic molecules.
Used in Drug Development:
3-IODO-2-METHOXYISONICOTINONITRILE is utilized in the development of new drugs due to its potential applications in medicinal chemistry. Its properties may contribute to the discovery of novel therapeutic agents with improved efficacy and selectivity.
Used in Material Science:
3-IODO-2-METHOXYISONICOTINONITRILE is employed in the field of material science for the development of new materials with unique properties. Its electron-withdrawing nature and structural features can be leveraged to create materials with specific characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 908279-57-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,2,7 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 908279-57:
(8*9)+(7*0)+(6*8)+(5*2)+(4*7)+(3*9)+(2*5)+(1*7)=202
202 % 10 = 2
So 908279-57-2 is a valid CAS Registry Number.
908279-57-2Relevant articles and documents
First total synthesis of Louisianin A
Chang, Ching-Yao,Liu, Hui-Ming,Chow, Tahsin J.
, p. 6302 - 6304 (2007/10/03)
The first total synthesis of louisianin A, 4-allyl-6,7-dihydro-1- hydroxycyclopenta[c]pyridin-5-one, is achieved from 2-chloro-4-cyanopyridine 5 via seven steps in an overall 24% yield. The key step is a cyclization- decarboxylation sequence toward the formation of a cyclopentenone ring.
