53279-73-5 Usage
Uses
Used in Organic Synthesis:
(2-HYDROXYMETHYL-4,5-DIIODO-PHENYL)-METHANOL is used as a building block in organic synthesis for the creation of various pharmaceuticals and biologically active molecules. Its unique structure allows for the development of new compounds with potential therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-HYDROXYMETHYL-4,5-DIIODO-PHENYL)-METHANOL is utilized as a key intermediate in the synthesis of pharmaceuticals. Its presence in the molecular structure can contribute to the desired biological activity and therapeutic effects of the final product.
Used in Dye Preparation:
(2-HYDROXYMETHYL-4,5-DIIODO-PHENYL)-METHANOL is also used in the preparation of dyes and other organic compounds. Its chemical properties make it suitable for the development of dyes with specific color characteristics and stability.
Used in Material Science:
In the field of material science, (2-HYDROXYMETHYL-4,5-DIIODO-PHENYL)-METHANOL has applications in the production of polymers and other organic materials. Its unique structure and properties can contribute to the development of new materials with improved performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 53279-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,7 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 53279-73:
(7*5)+(6*3)+(5*2)+(4*7)+(3*9)+(2*7)+(1*3)=135
135 % 10 = 5
So 53279-73-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H8I2O2/c9-7-1-5(3-11)6(4-12)2-8(7)10/h1-2,11-12H,3-4H2
53279-73-5Relevant academic research and scientific papers
Control of the molecular packing of chloroboron(III) and fluoroboron(III) subnaphthalocyanines by designing peripheral substituents
Takagi, Akuto,Mizutani, Tadashi
, p. 54235 - 54245 (2017/12/05)
Chloroboron(iii) and fluoroboron(iii) hexa(1-alkynyl)- and hexa(2-arylethynyl)subnaphthalocyanines with a large dipole moment were prepared by Sonogashira coupling of hexaiodosubnaphthalocyanines with substituted acetylenes. Introduction of butyl or longe
Synthesis and optoelectronic properties of hexachloro- and hexaiodosubnaphthalocyanines as organic electronic materials
Yamamoto, Koji,Takagi, Akuto,Hada, Miyako,Taniwaki, Ryosuke,Mizutani, Tadashi,Kimura, Yoshifumi,Takao, Yuko,Moriwaki, Kazuyuki,Matsumoto, Fukashi,Ito, Takatoshi,Iwai, Toshiyuki,Hida, Koichi,Mizuno, Takumi,Ohno, Toshinobu
, p. 4918 - 4924 (2016/07/18)
Chloroboron(III) hexachloro- and hexaiodosubnaphthalocyanines were prepared, and their solubility, electronic absorption spectroscopy, fluorescence emission spectroscopy and HOMO/LUMO energy levels were evaluated. These subnaphthalocyanines showed lower H
Design, synthesis, and properties of new derivatives of pentacene
Jiang, Jinyue,Kaafarani, Bilal R.,Neckers, Douglas C.
, p. 2155 - 2158 (2007/10/03)
Stable, soluble ethynylated derivatives of pentacene (9a-c) were synthesized, and the ethynyl moieties on the terminal rings were used to tune the electronic properties of these compounds. Their oxidation potentials are higher and their reduction potentia
