19403-92-0 Usage
Description
2,4,6-Triiodoresorcinol is an iodinated derivative of Resorcinol, a benzene derivative known for its keratolytic and antiseborrheic properties. It is characterized by the presence of three iodine atoms at the 2nd, 4th, and 6th positions of the resorcinol molecule, which contribute to its therapeutic effects.
Uses
Used in Dermatology:
2,4,6-Triiodoresorcinol is used as a keratolytic agent for promoting the shedding of the outer layers of the skin, particularly in conditions characterized by excessive keratinization, such as calluses, corns, and warts. Its ability to break down keratin helps in the treatment of various skin disorders.
Used in Veterinary Medicine:
In the veterinary field, 2,4,6-Triiodoresorcinol is used as a topical antipruritic to alleviate itching and discomfort in animals. It is also utilized as an antiseptic, particularly for its intestinal antiseptic properties, to help prevent and treat infections in the gastrointestinal tract of animals.
Used in Antiseptic Applications:
2,4,6-Triiodoresorcinol is employed as an antiseptic agent due to its ability to inhibit the growth of microorganisms, making it useful in the prevention and treatment of infections in both humans and animals. Its broad-spectrum antimicrobial activity contributes to its effectiveness in various medical and veterinary applications.
Check Digit Verification of cas no
The CAS Registry Mumber 19403-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,0 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 19403-92:
(7*1)+(6*9)+(5*4)+(4*0)+(3*3)+(2*9)+(1*2)=110
110 % 10 = 0
So 19403-92-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H3I3O2/c7-2-1-3(8)6(11)4(9)5(2)10/h1,10-11H
19403-92-0Relevant articles and documents
Isostructural polymorphs of triiodophloroglucinol and triiodoresorcinol
Nath, Naba K.,Saha, Binoy K.,Nangia, Ashwini
, p. 1693 - 1701 (2008)
Triiodoresorcinol (TIR, 2,4,6-triiodoresorcinol) and triiodophloroglucinol (TIG, 2,4,6-triiodophloroglucinol) crystallized as orthorhombic (TIR-O and TIG-O in P212121) and monoclinic (TIR-M and TIG-M in P21/n) p
A NEW ANTIVIRAL CHEMOTHERAPEUTANT, RIODOXOL
Grinev, A. N.,Pershin, G. N.,Stebaeva, L. F.,Nikolaeva, I. S.,Shvedov, V. I.,et al.
, p. 208 - 211 (1984)
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Iodination of anilines and phenols with 18-crown-6 supported ICl 2-
Mbatia, Hannah W.,Ulloa, Olbelina A.,Kennedy, Daniel P.,Incarvito, Christopher D.,Burdette, Shawn C.
experimental part, p. 2987 - 2991 (2011/06/16)
A highly crystalline iodinating reagent, {[K·18-C-6]ICl 2}n, was synthesized in high yield (93%). The trihalide is supported by an 18-crown-6 macrocycle and forms a coordination polymer in the solid state. This reagent iodinates anilines and phenols efficiently under mild conditions. Controlled mono-iodination with anilines was easily achieved while poly-iodination was observed with phenols.
Mild and efficient iodination of aromatic and heterocyclic compounds with the NaClO2/NaI/HCl system
Lista, Liliana,Pezzella, Alessandro,Napolitano, Alessandra,d'Ischia, Marco
, p. 234 - 239 (2008/09/16)
NaClO2/NaI in the presence of HCl is a mild, cheap, and non-toxic reagent for the iodination of phenols, including estradiol and naphthol, aromatic amines, and heterocyclic substrates, e.g., indoles, 8-hydroxyquinoline, imidazole, in fair to excellent yields by a very simple isolation protocol. The scope of the procedure is exemplified by the first iodination of 5-nitroindole to 3-iodo-5-nitroindole in 75% yield.
