19259-10-0 Usage
Uses
Used in Organic Chemistry:
2,3,5-Triiodothiophene is used as a building block for the synthesis of organic compounds, leveraging its high reactivity to participate in a wide range of chemical reactions. This application is crucial for the development of new materials and pharmaceuticals.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,3,5-Triiodothiophene is utilized as a key component in the creation of novel drugs. Its unique structure and reactivity allow for the design of compounds with specific therapeutic properties, contributing to advancements in medicinal chemistry.
Used in Material Science:
2,3,5-Triiodothiophene is also employed in material science for the development of functional materials. Its potential to form various chemical bonds and its structural characteristics make it a valuable component in the engineering of materials with tailored properties for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 19259-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,5 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19259-10:
(7*1)+(6*9)+(5*2)+(4*5)+(3*9)+(2*1)+(1*0)=120
120 % 10 = 0
So 19259-10-0 is a valid CAS Registry Number.
InChI:InChI=1/C4HI3S/c5-2-1-3(6)8-4(2)7/h1H
19259-10-0Relevant academic research and scientific papers
Selective metallation of 3-halothiophenes: Practical methods for the synthesis of 2-bromo-3-formylthiophene
Sonoda, Motohiro,Kinoshita, Shoko,Luu, Thanh,Fukuda, Hiroshi,Miki, Koji,Umeda, Rui,Tobe, Yoshito
experimental part, p. 3315 - 3323 (2011/03/20)
Selective lithiation of 3-bromothiophene was accomplished under controlled conditions without formation of undesired thienyllithium compounds. A thienyl Grignard reagent derived from 2-bromo-3-iodothiophene was transformed into 2-bromo-3-formylthiophene in high selectivity by formylation with dimethylformamide (DMF) at optimal reaction temperature. Copyright Taylor & Francis Group, LLC.
