6303-60-2 Usage
Uses
Used in Pharmaceutical Industry:
1,3-Diiodo-4-nitrobenzene is utilized as a building block for the synthesis of various pharmaceutical compounds. Its ability to introduce the 4-nitrophenyl iodide group into molecules is crucial for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 1,3-Diiodo-4-nitrobenzene serves as a key component in the synthesis of compounds used in agricultural chemicals, contributing to the creation of pesticides and other agrochemical products designed to enhance crop protection and yield.
Used in Research Laboratories:
1,3-Diiodo-4-nitrobenzene is also employed in research laboratories for its distinctive chemical properties and reactivity. It is instrumental in a variety of chemical reactions, providing researchers with a valuable tool for advancing scientific understanding and innovation in chemical synthesis.
It is imperative to handle 1,3-Diiodo-4-nitrobenzene with caution due to its toxic nature, ensuring that proper safety measures are implemented to prevent potential harm during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 6303-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6303-60:
(6*6)+(5*3)+(4*0)+(3*3)+(2*6)+(1*0)=72
72 % 10 = 2
So 6303-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H3I2NO2/c7-4-1-2-6(9(10)11)5(8)3-4/h1-3H
6303-60-2Relevant academic research and scientific papers
Catalysis and regioselectivity of the aqueous Heck reaction by Pd(0) nanoparticles under ultrasonic irradiation
Zhang, Zuhui,Zha, Zhenggen,Gan, Changsheng,Pan, Chongfeng,Zhou, Yuqing,Wang, Zhiyong,Zhou, Ming-Ming
, p. 4339 - 4342 (2007/10/03)
An aqueous Heck reaction carried out under ultrasonic irradiation at the ambient temperature (25 °C) has been shown in this study to afford high yields of corresponding products. It was found that as a catalyst for the reaction palladium forms nanoparticles in-situ, characterized by transmission electron microscopy (TEM) and X-ray powder diffraction (XRD) analyses, and can be recycled. Furthermore, the Heck reaction under such mild and environmentally friendly conditions offers excellent regioselectivity of para-over ortho-substitution in phenyl iodides especially with electron-donating groups.
