52107-82-1 Usage
Description
1-(2-iodo-5-methylphenyl)ethanone, a chemical compound with the molecular formula C9H9IO, is a yellow solid characterized by a melting point of 50-52°C. As a ketone derivative, it features a carbonyl group attached to two carbon atoms, and the presence of iodine and methyl groups in its structure endows it with unique reactivity, enabling a range of chemical reactions and applications. 1-(2-iodo-5-methylphenyl)ethanone is predominantly utilized in research and development laboratories for organic synthesis and serves as a fundamental building block for crafting more complex molecules.
Uses
Used in Pharmaceutical Synthesis:
1-(2-iodo-5-methylphenyl)ethanone is used as an intermediate in the pharmaceutical industry for the synthesis of various organic compounds. Its unique reactivity and structural features make it a valuable component in the development of new drugs and medicinal agents.
Used in Agrochemical Production:
In the agrochemical industry, 1-(2-iodo-5-methylphenyl)ethanone is employed as an intermediate for synthesizing a range of agrochemicals. Its role in creating complex molecules contributes to the development of innovative products for agricultural applications.
Used in Research and Development Laboratories:
1-(2-iodo-5-methylphenyl)ethanone is also used in research and development laboratories, where it serves as a key component in organic synthesis. Its unique properties and reactivity make it an essential tool for creating new and complex molecules for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 52107-82-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,0 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52107-82:
(7*5)+(6*2)+(5*1)+(4*0)+(3*7)+(2*8)+(1*2)=91
91 % 10 = 1
So 52107-82-1 is a valid CAS Registry Number.
52107-82-1Relevant articles and documents
Palladium-Catalyzed Alkylation with Alkyl Halides by C(sp3)?H Activation
Wu, Zhuo,Ma, Ding,Zhou, Bo,Ji, Xiaoming,Ma, Xiaotian,Wang, Xiaoling,Zhang, Yanghui
supporting information, p. 12288 - 12291 (2017/09/06)
Utilizing halogens as traceless directing goups represents an attractive strategy for C?H functionalization. A two C?H alkylation system, initiated by the oxidative addition of organohalides to Pd0, has been developed. The first reaction involves an intermolecular alkylation of palladacycles to form C(sp3)?C(sp2) bonds followed by C(sp2)?H activation/cyclization to deliver alkylated benzocyclobutenes as the final products. In the second reaction, two C?C bonds are formed by the reaction of palladacycles with CH2Br2, and provides a facile and efficient method for the synthesis of indanes. The alkylated benzocyclobutene products can be transformed into tricyclic hyrocarbons, and the indane derivatives are essential structural motifs in bioactive and odorant molecules.
