84483-30-7 Usage
Uses
Used in Organic Synthesis:
4-amino-3,5-dibromoacetanilide is used as an intermediate in the production of pharmaceuticals, dyes, and other organic compounds, playing a pivotal role in the synthesis of a wide array of chemical entities.
Used in Pharmaceutical Production:
As a key component in the development of new pharmaceuticals, 4-amino-3,5-dibromoacetanilide is utilized for its ability to contribute to the formation of medicinally relevant molecules.
Used in Dye Manufacturing:
4-amino-3,5-dibromoacetanilide is also employed in the production of dyes, where its chemical properties contribute to the color and stability of the final product.
Used as a Reagent in Organic Chemistry Reactions:
4-amino-3,5-dibromoacetanilide serves as a reagent in various organic chemistry reactions, particularly in the synthesis of heterocyclic compounds and pharmaceuticals, facilitating the creation of complex molecular structures.
Used in Antifungal and Antimicrobial Applications:
4-amino-3,5-dibromoacetanilide has been studied for its potential as an antifungal and antimicrobial agent, indicating its use in the development of treatments for fungal and bacterial infections.
Used in Research and Development:
In the pharmaceutical and chemical research sectors, 4-amino-3,5-dibromoacetanilide is used to explore new avenues in drug discovery and the synthesis of novel compounds with therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 84483-30-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,4,8 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84483-30:
(7*8)+(6*4)+(5*4)+(4*8)+(3*3)+(2*3)+(1*0)=147
147 % 10 = 7
So 84483-30-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H8Br2N2O/c1-4(13)12-5-2-6(9)8(11)7(10)3-5/h2-3H,11H2,1H3,(H,12,13)
84483-30-7Relevant academic research and scientific papers
Doddamani, Radha V.,Rachipudi, Padmeshwary S.,Pattanashetti, Nandini A.,Kariduraganavar, Mahadevappa Y.
, p. 15723 - 15735 (2019)
This paper emphasizes the preparation of nonlinear optical (NLO) responsive chromophores and their corresponding polymers. Initially, the carboxyl acid group-based precursors of the chromophores containing strong acceptors such as nitro-substituted thiazo
