128071-77-2 Usage
Uses
Used in Scientific Research:
4-Bromo-2-fluoropyridine-3-carboxaldehyde is used as a key intermediate in the synthesis of various complex compounds, particularly in the field of organic chemistry. Its unique structure and reactivity make it a valuable building block for creating new molecules with potential applications in pharmaceuticals, materials science, and other areas of research.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-Bromo-2-fluoropyridine-3-carboxaldehyde is used as a starting material for the development of new drugs. Its structural features allow for the creation of novel molecules with potential therapeutic properties, contributing to the advancement of medicine and the treatment of various diseases.
Used in Materials Science:
4-Bromo-2-fluoropyridine-3-carboxaldehyde is employed as a component in the synthesis of advanced materials, such as polymers and composites, with unique properties. Its incorporation into these materials can lead to improved performance characteristics, such as enhanced stability, reactivity, or selectivity, making it a valuable asset in the development of new materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 128071-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,0,7 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 128071-77:
(8*1)+(7*2)+(6*8)+(5*0)+(4*7)+(3*1)+(2*7)+(1*7)=122
122 % 10 = 2
So 128071-77-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrFNO/c7-5-1-2-9-6(8)4(5)3-10/h1-3H
128071-77-2Relevant academic research and scientific papers
Migration du lithium en serie pyridinique: double catalyse et reformage. Acces aux derives de la bromo-2 lithio-3 pyridine et des bromo-4 halogeno-2 lithio-3 pyridines
Mallet, Marc,Branger, Gilles,Marsais, Francis,Queguiner, Guy
, p. 319 - 332 (2007/10/02)
The lithium of an organolithium-pyridinic derivative can be moved from one position to an another by an intermolecular reaction.Two new reactions are possible for pyridinic organic synthesis: the isomerisation of any lithio derivative to a more stable one, and a reaction that transforms a mixture of various bromo-lithio derivatives into a single one.The processes involved and the experimental tools used are described in terms of the 2-bromo-3-lithio- and 4-bromo-2-halogeno-3-lithiopyridines derivatives synthesis.
