16488-60-1 Usage
Description
2,5-Diiodo-3-methylthiophene is a chemical compound with the molecular formula C5H4I2S. It is a derivative of thiophene, featuring a five-membered aromatic ring with one sulfur atom. Characterized by the presence of two iodine atoms and a methyl group attached to the thiophene ring, this compound is known for its unique structure and reactivity, making it a valuable building block in various applications.
Uses
Used in Organic Synthesis:
2,5-Diiodo-3-methylthiophene is used as a building block in organic synthesis for its unique reactivity and structural properties. It serves as a key intermediate in the production of various compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5-Diiodo-3-methylthiophene is used as a precursor for the development of new pharmaceuticals. Its unique structure allows for the creation of novel compounds with potential therapeutic applications.
Used in Agrochemical Industry:
2,5-Diiodo-3-methylthiophene is also utilized as a starting material in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Materials Science:
In the field of materials science, 2,5-Diiodo-3-methylthiophene is employed in the development of new materials with specific properties, such as electronic or optical characteristics, due to its unique molecular structure.
Check Digit Verification of cas no
The CAS Registry Mumber 16488-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,8 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16488-60:
(7*1)+(6*6)+(5*4)+(4*8)+(3*8)+(2*6)+(1*0)=131
131 % 10 = 1
So 16488-60-1 is a valid CAS Registry Number.
16488-60-1Relevant articles and documents
Method for synthesizing mono-aryl iodide or di-aryl iodide based on aromatic hydrocarbon carboxylic acid decarboxylic reaction
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Paragraph 0093; 0094, (2017/07/23)
The invention discloses a method for synthesizing mono-aryl iodide or di-aryl iodide based on aromatic hydrocarbon carboxylic acid decarboxylic reaction. The method is characterized in that under a protective atmosphere, carrying out one-pot reaction on a
Halogenation Using Quaternary Ammonium Polyhalides. XXXI. Halogenation of Thiophene Derivatives with Benzyltrimethylammonium Polyhalides
Okamoto, Tsuyoshi,Kakinami, Takaaki,Fujimoto, Hiroshi,Kajigaeshi, Shoji
, p. 2566 - 2568 (2007/10/02)
The reactions of thiophene derivatives with benzyltrimethylammonium tetrachloroiodate, benzyltrimethylammonium tribromide, and benzyltrimethylammonium dichloroiodate in acetic acid or in acetic acid-zinc chloride under mild conditions gave chloro-, bromo-, and iodo-substituted thiophene derivatives, respectively, in satifactory yields.
