35736-52-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4-dibromo-5-methoxyaniline is utilized as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules with specific therapeutic properties, contributing to the development of novel treatments for a range of medical conditions.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 2,4-dibromo-5-methoxyaniline serves as a valuable building block for the synthesis of complex organic compounds. Its reactivity with other chemical entities enables the formation of a wide array of molecules with diverse applications in various industries.
Used in Materials Science Research:
2,4-dibromo-5-methoxyaniline has been studied for its potential applications in materials science. Its unique chemical structure and properties make it a candidate for the development of new materials with specific characteristics, such as improved stability, reactivity, or other desirable traits.
Used in Organic Chemistry Research:
As a compound with distinct chemical properties, 2,4-dibromo-5-methoxyaniline is employed in organic chemistry research to explore new reaction pathways, mechanisms, and the synthesis of novel organic molecules. Its reactivity and structural features provide a foundation for advancing the understanding of organic chemical processes.
Safety Precautions:
Due to the reactivity of 2,4-dibromo-5-methoxyaniline and potential health hazards associated with its use, it is crucial to follow proper handling and safety protocols when working with 2,4-dibromo-5-methoxyaniline. This includes the use of appropriate personal protective equipment, working in well-ventilated areas, and adhering to established safety guidelines to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 35736-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,3 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35736-52:
(7*3)+(6*5)+(5*7)+(4*3)+(3*6)+(2*5)+(1*2)=128
128 % 10 = 8
So 35736-52-8 is a valid CAS Registry Number.
35736-52-8Relevant academic research and scientific papers
Synthesis and reactivity of dimethoxy-functionalised Troeger's base analogues
Malik, Qasim M.,Ijaz, Sadia,Craig, Donald C.,Try, Andrew C.
experimental part, p. 5798 - 5805 (2011/08/21)
Troeger's base analogues were prepared bearing methoxy groups in the 1,7-, 2,8-, 3,9- or 4,10-positions. These compounds were converted to their dihydroxy analogues in excellent yields upon treatment with boron tribromide and the 4,10-dihydroxy analogue could be prepared by directly from 4-hydroxyaniline. The synthetic utility of the dihydroxy-functionalised compounds as building blocks was demonstrated by the synthesis of a dialkoxy and a diester Troeger's base analogue.
Effect of structural factors and solvent nature in bromination of anilines
Bagmanov
experimental part, p. 1570 - 1576 (2011/06/20)
Reaction of electrophilic bromination of aniline containing various ortho, meta, and para substituents in the aromatic ring was studied. The optimal conditions for synthesis of mono-, di-, tri-, and tetrabromo derivatives of aniline and brominated analog of Aniline Black were found.
Polymer-supported organotin reagents for regioselective halogenation of aromatic amines
Chretien, Jean-Mathieu,Zammattio, Francoise,Le Grognec, Erwan,Paris, Michael,Cahingt, Blanche,Montavon, Gilles,Quintard, Jean-Paul
, p. 2870 - 2873 (2007/10/03)
(Chemical Equation Presented) Polymer-supported triorganotin halides were used in the halogenation reaction of aromatic amines. Treatment of aromatic amines with n-butyllithium and polymer-supported organotin halides gave the corresponding polymer-bound N-triorganostannylamines, which by treatment with bromine or iodine monochloride gave the para-halogenated aromatic amines with high yields and high selectivities. The polymer-supported organotin halides reagents regenerated during the course of the halogenation reaction can be reused without loss of efficiency. The presence of tin residues in halogenated aromatic amines was also investigated and evaluated at under 20 ppm after three runs.
