798552-96-2 Usage
Uses
Used in Pharmaceutical Industry:
2,4-dibromo-5-iodotoluene is used as an intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex organic molecules, contributing to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-dibromo-5-iodotoluene serves as an intermediate in the production of agrochemicals, aiding in the creation of compounds that can be used in pest control and crop protection.
Used in Organic Synthesis:
2,4-dibromo-5-iodotoluene is utilized as a reagent in palladium-catalyzed cross-coupling reactions, a key technique in organic chemistry for forming carbon-carbon bonds, which is essential for constructing a wide range of organic compounds.
Used in Research and Development:
As a building block in the development of various organic compounds, 2,4-dibromo-5-iodotoluene is employed in research and development settings to explore new chemical pathways and synthesize novel compounds with potential applications in various fields.
It is crucial to handle 2,4-dibromo-5-iodotoluene with care due to its potential hazards if ingested, inhaled, or comes into contact with the skin, and appropriate safety measures should be strictly followed during its use.
Check Digit Verification of cas no
The CAS Registry Mumber 798552-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,8,5,5 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 798552-96:
(8*7)+(7*9)+(6*8)+(5*5)+(4*5)+(3*2)+(2*9)+(1*6)=242
242 % 10 = 2
So 798552-96-2 is a valid CAS Registry Number.
798552-96-2Relevant academic research and scientific papers
Tae, Woo Kim,Kool, Eric T.
, p. 3949 - 3952 (2004)
(Chemical Equation Presented) We describe a series of nonpolar nucleoside analogues having similar shapes and gradually increasing size. The structure of the nucleobase thymine was mimicked with toluene derivatives, replacing 02/04 with hydrogen, fluorine, chlorine, bromine, and iodine. Glycosidic bonds were formed by reactions of lithiated 2,4-dihalotoluenes with a deoxyribonolactone derivative. Structural analysis by NMR showed similar conformations across the series. The compounds are useful for study of the biological recognition of nucleotides and nucleic acids.
