90003-93-3 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4-DIMETHYL-6-IODOPHENOL is used as a chemical intermediate for the production of various pharmaceuticals and organic compounds. Its unique structure with iodine and methyl groups allows for versatile reactions and modifications, contributing to the synthesis of a wide range of medicinal agents.
Used in Antimicrobial Research:
In the field of medicine and biotechnology, 2,4-DIMETHYL-6-IODOPHENOL is used as a subject of study for its potential antifungal and antibacterial properties. Its ability to inhibit the growth of certain microorganisms makes it a valuable candidate for the development of new antimicrobial agents, particularly in an era where resistance to existing antibiotics is increasing.
Used in Chemical Research and Development:
2,4-DIMETHYL-6-IODOPHENOL is also utilized in chemical research and development for its potential applications in creating new compounds with specific properties. Its reactivity and structural features make it a useful building block in the design and synthesis of novel organic molecules for various applications, including but not limited to, materials science, agrochemicals, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 90003-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,0 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90003-93:
(7*9)+(6*0)+(5*0)+(4*0)+(3*3)+(2*9)+(1*3)=93
93 % 10 = 3
So 90003-93-3 is a valid CAS Registry Number.
90003-93-3Relevant articles and documents
Gold-catalyzed oxidative acyloxylation of arenes
Pradal, Alexandre,Toullec, Patrick Y.,Michelet, Veronique
experimental part, p. 6086 - 6089 (2011/12/22)
A variety of nonactivated hindered aromatic rings are acyloxylated (22 examples, up to 83% yield) in the presence of PPh3AuCl as the catalyst and di(acetoxy)iodobenzene as the oxidant. The reaction proceeds at 110 °C in an acid media and allows the formation of both hindered acetoxy and acyloxy derivatives. This methodology nicely complements the Pd-catalyzed arene acyloxylation reaction, which is not operating on hindered substrates and allows the Au-catalyzed unprecedented acyloxylation reaction of arenes, implying various carboxylic acids.
