5503-82-2 Usage
Uses
Used in Organic Synthesis:
1,2-Diiodo-3,4,5,6-tetramethylbenzene is used as a reagent in organic synthesis for the preparation of a wide range of organic compounds. Its unique structure and reactivity make it a valuable component in creating diverse chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1,2-Diiodo-3,4,5,6-tetramethylbenzene is used as a key intermediate in the synthesis of various drugs. Its presence in the production process aids in the development of new medicinal compounds with potential therapeutic applications.
Used in Dye Manufacturing:
1,2-Diiodo-3,4,5,6-tetramethylbenzene is also utilized in the production of dyes, where its chemical properties contribute to the creation of vibrant and stable colorants for various applications.
Used in Industrial Product Development:
Beyond pharmaceuticals and dyes, 1,2-Diiodo-3,4,5,6-tetramethylbenzene finds use in the development of other industrial products, capitalizing on its reactive nature to form new compounds with specific properties for specialized applications.
Safety Note:
Due to its high reactivity and potential hazards, 1,2-Diiodo-3,4,5,6-tetramethylbenzene should be handled with extreme caution. Proper safety measures, including the use of personal protective equipment and adherence to safety protocols, are essential when working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 5503-82-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,0 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5503-82:
(6*5)+(5*5)+(4*0)+(3*3)+(2*8)+(1*2)=82
82 % 10 = 2
So 5503-82-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H12I2/c1-5-6(2)8(4)10(12)9(11)7(5)3/h1-4H3
5503-82-2Relevant academic research and scientific papers
Synthesis of annulated dioxins as electron-rich donors for cation radical salts
Hellberg, Jonas,Dahlstedt, Emma,Pelcman, Margit E.
, p. 8899 - 8912 (2007/10/03)
The synthesis of a series of new alkoxylated linearly annulated dioxins is described together with their cyclic voltammetric behavior and some preliminary result on their ability to form cation radical salts. Of these dioxins, seven (8, 12, 19, 21, 27, 33, 34) are the first representatives of entirely new heterocyclic systems. Dioxins 8, 21, 22 and 27 gave good quality cation radical salts upon electrocrystallization. Graphical Abstract
Selective and effective iodination of alkyl-substituted benzenes with elemental iodine activated by Selectfluor F-TEDA-BF4
Stavber, Stojan,Kralj, Petra,Zupan, Marko
, p. 598 - 600 (2007/10/03)
Selective direct introduction of an iodine atom into alkyl-substituted benzene derivatives was effectively achieved by reaction of target molecules with elemental iodine in the presence of 1-chloromethyl-4-fluoro- 1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) (Selectfluor F-TEDA-BF4). The number of iodine atoms introduced could be modulated by the molar ratio between substrate, iodine and F-TEDA-BF4.
Halogenation Using Quaternary Ammonium Polyhalides. XIV. Aromatic Bromination and Iodination of Arenes by Use of Benzyltrimethylammonium Polyhalides-Zinc Chloride System
Kajigaeshi, Shoji,Kakinami, Takaaki,Moriwaki, Masayuki,Tanaka, Toshio,Fujisaki, Shizuo,Okamoto, Tsuyoshi
, p. 439 - 443 (2007/10/02)
The reaction of arenes with benzyltrimethylammonium tribromide or benzyltrimethylammonium dichloroiodate in acetic acid in the presence of ZnCl2 at room temperature or at 70 deg C gave brome- or iodo-substituted arenes in good yield, respectively.
