42860-06-0 Usage
Uses
Used in Organic Synthesis:
4-bromo-3-iodobenzoic acid is used as a building block in organic synthesis for the preparation of various biologically active molecules. Its bromine and iodine substituents enable it to undergo cross-coupling reactions, allowing the formation of complex molecular structures with potential applications in various fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-bromo-3-iodobenzoic acid is utilized as a key intermediate for the synthesis of pharmaceutical compounds. Its unique structural features and reactivity make it a valuable component in the development of new drugs with improved therapeutic properties.
Used in Research and Development:
4-bromo-3-iodobenzoic acid is employed as a starting material in research and development for the synthesis of new pharmaceuticals, agrochemicals, and materials science applications. Its potential pharmacological properties and ability to form complex molecular structures make it an attractive candidate for further exploration and innovation in these industries.
Check Digit Verification of cas no
The CAS Registry Mumber 42860-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,8,6 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 42860-06:
(7*4)+(6*2)+(5*8)+(4*6)+(3*0)+(2*0)+(1*6)=110
110 % 10 = 0
So 42860-06-0 is a valid CAS Registry Number.
42860-06-0Relevant academic research and scientific papers
Oxidative iodination of deactivated arenes in concentrated sulfuric acid with I2/NaIO4 and KI/NaIO4 iodinating systems
Kraszkiewicz, Lukasz,Sosnowski, Maciej,Skulski, Lech
, p. 1195 - 1199 (2007/10/03)
Deactivated arenes were mono- or diiodinated with strong electrophilic I+ reagents, which were prepared from NaIO4 and either I2 or KI in concentrated H2SO4 (minimum 95% by weight). In general a small excess of the dark brown iodinating solution was used (1.1/1.5 equivalents, for nitrobenzene two equivalents was required). The iodinations were conducted at 25-30 °C with a reaction time of 1-2 hours using either a 'direct' or an 'inverse' method of aromatic iodination to give mono- or diiodinated pure products in 31-91% optimized yields. Georg Thieme Verlag Stuttgart.
