150908-00-2 Usage
Description
3-Bromo-2-iodo-phenylamine is a chemical compound with the molecular formula C6H5BrIN. It is a derivative of phenylamine and contains both a bromine and iodine atom attached to the phenyl ring. 3-Bromo-2-iodo-phenylamine is known for its potential applications in various fields due to its unique structure and properties.
Uses
Used in Organic Synthesis:
3-Bromo-2-iodo-phenylamine is used as a building block in organic synthesis for the creation of more complex molecules. Its presence of both bromine and iodine atoms allows for versatile chemical reactions, making it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Research:
In pharmaceutical research, 3-Bromo-2-iodo-phenylamine is utilized as a key intermediate for the development of new drugs. Its unique structure contributes to the design and synthesis of pharmaceuticals with potential therapeutic effects.
Used in Agrochemicals:
3-Bromo-2-iodo-phenylamine is also used as a reagent in the synthesis of agrochemicals. Its role in this industry is crucial for the development of effective pesticides and other agricultural products that can protect crops and enhance agricultural productivity.
Used in Biological and Medicinal Studies:
Although further research is needed, 3-Bromo-2-iodo-phenylamine has been studied for its potential biological and medicinal properties. Its unique chemical structure may offer new avenues for the treatment of various diseases and conditions, making it a promising candidate for future medical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 150908-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,9,0 and 8 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 150908-00:
(8*1)+(7*5)+(6*0)+(5*9)+(4*0)+(3*8)+(2*0)+(1*0)=112
112 % 10 = 2
So 150908-00-2 is a valid CAS Registry Number.
150908-00-2Relevant articles and documents
Construction of Tricyclic Nitrogen Heterocycles by a Gold(I)-Catalyzed Cascade Cyclization of Allenynes and Application to Polycyclic π-Electron Systems
Arichi, Norihito,Fukazawa, Aiko,Ikeuchi, Takaya,Inuki, Shinsuke,Komatsu, Hiroki,Ohno, Hiroaki,Oishi, Shinya,Tsuno, Hitomi,Yasui, Kosuke
supporting information, p. 27019 - 27025 (2021/11/27)
A novel approach to the direct construction of tricyclic nitrogen heterocycles based on gold-catalyzed cascade cyclization of aminoallenynes is described. The expected biscyclization reaction of hydroxyisobutyryl-protected aminoallenynes was efficiently promoted by a catalytic amount of BrettPhosAuNTf2 in the presence of iPrOH to produce 1,2-dihydrobenzo[cd]indole derivatives in good yields. When the reaction was combined with Friedel–Crafts acylation or palladium-catalyzed N-arylation, the resulting tricyclic products were efficiently converted into nitrogen-containing polycyclic aromatic compounds (N-PACs) with highly conjugated π-electron systems. A newly obtained hexacyclic indolium salt showed characteristic concentration-dependent absorption and emission properties.
