64085-53-6 Usage
Uses
Used in Organic Synthesis:
2,5-DIIODOANILINE is used as a reagent in organic synthesis for its strong nucleophilic properties, facilitating the formation of carbon-carbon bonds and contributing to the creation of a wide range of chemical compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 2,5-DIIODOANILINE is employed as a key intermediate in the synthesis of various drugs, leveraging its reactivity to form essential molecular structures within medicinal compounds.
Used in Dye Production:
2,5-DIIODOANILINE is utilized as a precursor in the production of dyes, where its chemical structure contributes to the color properties and stability of the final dye products.
Used in Agrochemicals:
2,5-DIIODOANILINE serves as a reagent in the synthesis of agrochemicals, playing a role in the development of pesticides and other agricultural chemicals to improve crop protection and yield.
Used in Plastics and Polyurethane Production:
This chemical compound is also used in the manufacturing process of certain types of plastics and polyurethane, where its unique properties contribute to the material's characteristics, such as durability and flexibility.
Check Digit Verification of cas no
The CAS Registry Mumber 64085-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64085-53:
(7*6)+(6*4)+(5*0)+(4*8)+(3*5)+(2*5)+(1*3)=126
126 % 10 = 6
So 64085-53-6 is a valid CAS Registry Number.
64085-53-6Relevant academic research and scientific papers
NaIO4/KI/NaCl: a new reagent system for iodination of activated aromatics through in situ generation of iodine monochloride
Emmanuvel, Lourdusamy,Shukla, Ravi Kant,Sudalai, Arumugam,Gurunath, Suryavanshi,Sivaram, Swaminathan
, p. 4793 - 4796 (2007/10/03)
A new reagent system consisting of NaIO4/KI/NaCl in aq AcOH has been found to be effective in iodinating a variety of activated aromatic substrates via in situ-generated iodine monochloride, to furnish iodoaromatics in excellent yields. This iodination procedure has been applied successfully for a cost-effective synthesis of 3,3′-diaminobenzidine, a key intermediate for preparing proton conducting membranes for fuel cell applications, with high yield and a purity of 99.7%.
