4102-54-9 Usage
Description
2,4-DIMETHYL-6-IODOANILINE is an organic compound with the molecular formula C8H10IN. It is characterized by the presence of two methyl groups at the 2nd and 4th positions and an iodine atom at the 6th position on the aniline backbone. 2,4-DIMETHYL-6-IODOANILINE is known for its chemical reactivity and is often utilized in various synthetic applications.
Uses
Used in Chemical Synthesis:
2,4-DIMETHYL-6-IODOANILINE is used as a synthetic intermediate for the production of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable building block in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,4-DIMETHYL-6-IODOANILINE is used as a key component in the development of new drugs. Its chemical properties enable it to be incorporated into the structures of potential therapeutic agents, contributing to their overall efficacy and pharmacological properties.
Used in Dye Manufacturing:
2,4-DIMETHYL-6-IODOANILINE is also employed in the manufacturing of dyes, particularly those with specific color properties. Its ability to form various chemical bonds and its reactivity make it a suitable candidate for the production of dyes with unique characteristics.
Used in Research and Development:
Due to its versatile chemical properties, 2,4-DIMETHYL-6-IODOANILINE is often utilized in research and development settings. Scientists and researchers use this compound to explore new reaction pathways, develop novel synthetic methods, and investigate its potential applications in various fields.
Used in the Synthesis of Benzothiazoles:
2,4-DIMETHYL-6-IODOANILINE is used as a reactant in the synthesis of benzothiazoles through copper-catalyzed one-pot three-component reactions, with sodium hydrosulfide serving as a sulfur surrogate. This application highlights the compound's role in the creation of complex and valuable chemical structures.
Check Digit Verification of cas no
The CAS Registry Mumber 4102-54-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4102-54:
(6*4)+(5*1)+(4*0)+(3*2)+(2*5)+(1*4)=49
49 % 10 = 9
So 4102-54-9 is a valid CAS Registry Number.
4102-54-9Relevant articles and documents
Synthesis, structure, and heck cyclization of the syn- and anti-atropisomers of N-acyl-N-(4-methyl-3,6-dihydro-2H-pyran-3-yl)-2-iodo-4,6- dimethylaniline
Skladchikov,Suponitskii,Gataullin
, p. 1486 - 1490 (2013)
The reaction of 2-iodo-2,4-dimethylaniline with 3,4-dibromo-4- methyltetrahydro-2H-pyran, followed by treatment with acetyl bromide or 4-nitrobenzoyl chloride, gave syn- and anti-atropisomers of N-(2-iodo-4,6- dimethylphenyl)-N-(4-methyl-3,6-dihydro-2H-py
A Diastereoselective Route to Benzoannelated Bridged Sultams
Klochkova, Anastasiia A.,Rassadin, Valentin A.,Sokolov, Victor V.
supporting information, p. 4484 - 4494 (2021/08/13)
A practical diastereoselective method for the synthesis of benzoannelated tri- and tetracyclic bridged sultams has been developed. The synthetic route employs widely available, substituted -iodoanilines and is based on intramolecular Michael addition followed by cycloalkylation with dihaloalkanes, or vice versa. The target compounds were isolated in good yields and the diastereoselectivity of the reaction could be easily controlled by the order of Michael addition and cycloalkylation steps.
Method for preparing o-haloaromaticamine from C-H-based activated arylamines
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Paragraph 0049; 0050; 0051; 0052; 0053, (2017/07/22)
The invention belongs to the technical field of organic chemistry and particularly relates to a method for preparing o-haloaromaticamine from C-H-based activated arylamines. The method comprises the following steps: taking anhydrous copper acetate as a reaction catalyst and hydrogen peroxide as an oxidizing agent, adding aniline compounds and potassium bromide or potassium iodide into water for reaction at room temperature for 2 h, extracting with ethyl acetate and concentrating under reduced pressure, so as to obtain a corresponding arylamine halogenated compound crude product; and performing column chromatographic isolation and purification to obtain a corresponding purified product. The method has the characteristics that the operation is simple, reaction conditions are mild, the reaction time is short, and the method is environment-friendly.