84483-28-3 Usage
Uses
Used in Pharmaceutical Industry:
2-Chloro-6-iodoaniline serves as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of diverse molecular entities with potential medicinal properties.
Used in Organic Chemistry:
In the field of organic chemistry, 2-Chloro-6-iodoaniline is utilized as a building block for the synthesis of complex organic molecules. Its presence of both chlorine and iodine atoms enables further functionalization and modification, leading to the formation of a wide range of chemical compounds.
Used in Dye and Pigment Production:
2-Chloro-6-iodoaniline is employed in the production of dyes and pigments due to its ability to impart color to various substrates. Its chemical structure allows for the creation of stable and vibrant colorants used in industries such as textiles, plastics, and printing inks.
Safety Measures:
Given its potentially hazardous nature, 2-Chloro-6-iodoaniline should be handled and stored with appropriate safety measures. This includes the use of personal protective equipment, proper ventilation, and adherence to established safety protocols to minimize the risk of exposure and ensure the well-being of individuals working with 2-Chloro-6-iodoaniline.
Check Digit Verification of cas no
The CAS Registry Mumber 84483-28-3 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, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 84483-28:
(7*8)+(6*4)+(5*4)+(4*8)+(3*3)+(2*2)+(1*8)=153
153 % 10 = 3
So 84483-28-3 is a valid CAS Registry Number.
84483-28-3Relevant academic research and scientific papers
Synthesis and Investigation of the Abiotic Formation of Pyonitrins A-D
Aniebok, Victor,Lee, Hsiau-Wei,Macmillan, John B.,Shingare, Rahul D.
supporting information, (2020/02/22)
Pyonitrins A-D are recently isolated natural products from the insect-associated Pseudomonas protegens strain, which were isolated from complex fractions that exhibited antifungal activity via an in vivo murine candidiasis assay. Genomic studies of Pseudomonas protegens suggested that pyonitrins A-D are formed via a spontaneous nonenzymatic reaction between biosynthetic intermediates of two well-known natural products pyochelin and pyrrolnitrin. Herein we have accomplished the first biomimetic total synthesis of pyonitrins A-D in three steps and studied the nonenzymatic formation of the pyonitrins using 15N NMR spectroscopy.
Selective reduction of halogenated nitroarenes with hydrazine hydrate in the presence of Pd/C
Li, Fang,Frett, Brendan,Li, Hong-Yu
, p. 1403 - 1408 (2014/06/23)
A large variety of halogenated nitroarenes have been selectively reduced with hydrazine hydrate in the presence of Pd/C to give the corresponding (halogenated) anilines in good yield.
