408359-07-9 Usage
Uses
Used in Organic Synthesis:
3-Bromo-2-formylpyrrole is used as a building block for the synthesis of various functionalized pyrrole derivatives. Its unique structure and reactivity allow it to undergo a range of chemical reactions, such as nucleophilic substitution and condensation, making it a versatile component in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
3-Bromo-2-formylpyrrole is used as a key intermediate in the development of pharmaceutical products. Its ability to participate in various chemical reactions enables the synthesis of a wide array of bioactive compounds with potential therapeutic applications.
Used in Agrochemical Industry:
3-Bromo-2-formylpyrrole is also utilized in the agrochemical sector as an intermediate for the synthesis of agrochemical products. Its diverse reactivity contributes to the development of new compounds with pesticidal or herbicidal properties, enhancing crop protection and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 408359-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,8,3,5 and 9 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 408359-07:
(8*4)+(7*0)+(6*8)+(5*3)+(4*5)+(3*9)+(2*0)+(1*7)=149
149 % 10 = 9
So 408359-07-9 is a valid CAS Registry Number.
408359-07-9Relevant academic research and scientific papers
Studies of palladium-catalyzed coupling reactions for preparation of hindered 3-arylpyrroles relevant to (-)-rhazinilam and its analogues
Ghosez, Leon,Franc, Cecile,Denonne, Frederic,Cuisinier, Claire,Touillaux, Roland
, p. 1827 - 1839 (2007/10/03)
Suzuki cross-coupling reactions of 3-pyrroleboronic acid derivatives with haloaromatics and the reverse process i.e., the coupling of 3-iodo(bromo)pyrroles with arylboronic acids have been investigated as a potential key step in the synthesis of (-)-rhazinilam and analogues. It was found that 3-iodo-2-formyl-1-tosylpyrroles efficiently coupled with a variety of arylboronic acids in the presence of PdCl2(dppf) as catalyst. This catalytic system is compatible with a broad spectrum of arylboronic acids - electron-rich, electron-poor, hindered, heterocyclic - which easily coupled with the pyrrole substrate.
