57841-90-4 Usage
Uses
Used in Chemical Reactions:
3-IODO-N-PHENYL-2-PYRIDINECARBOXAMIDE is used as a reactive compound for various chemical reactions due to its unique structure and properties. The presence of the Iodine atom makes it a good candidate for iodination reactions, while the Pyridine and Phenyl rings allow it to participate in a range of aromatic reactions.
Used in Pharmaceutical Research:
3-IODO-N-PHENYL-2-PYRIDINECARBOXAMIDE is used as a potential candidate in pharmaceutical research for the development of new drugs. Its chemical structure and reactivity may offer opportunities for the synthesis of novel compounds with potential therapeutic applications.
Used in Material Science:
3-IODO-N-PHENYL-2-PYRIDINECARBOXAMIDE is used as a building block in the synthesis of new materials with specific properties. The combination of the Iodine atom, Pyridine ring, and Phenyl ring may contribute to the creation of materials with unique electronic, optical, or mechanical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 57841-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,4 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57841-90:
(7*5)+(6*7)+(5*8)+(4*4)+(3*1)+(2*9)+(1*0)=154
154 % 10 = 4
So 57841-90-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H9IN2O/c13-10-7-4-8-14-11(10)12(16)15-9-5-2-1-3-6-9/h1-8H,(H,15,16)
57841-90-4Relevant articles and documents
Synthesis of santiagonamine
Markey, Michael D.,Ying, Fu,Kelly, T. Ross
, p. 3255 - 3257 (2008/02/11)
The first total synthesis of santiagonamine (1) is achieved in 12 steps from isovanillin. A palladium-catalyzed Ullmann cross-coupling reaction and a photocyclization are the key steps in the synthesis.
Application of organolithium compounds in organic synthesis. Part 19. Synthetic strategies based on aromatic metallation. A concise regiospecific synthesis of 3-halogenated picolinic and isonicotinic acids
Epsztajn,Plotka,Grabowska
, p. 1075 - 1086 (2007/10/03)
The synthesis of the halogenated picolin- and isonicotinalides (3) and (4) via metallation (n-BuLi) of the anilides (1) and (2) and then the reaction of the generated bis-lithiated anilides with halogenating agents (CCl3-CCl3, CH2Br-CH2Br, I2) followed by subsequent acidic hydrolysis of (3) and (4), as a way of regiospecific transformation of picoline and isonicotine acids into their C3-halogenated derivatives, is described.
