718615-92-0 Usage
Description
Thieno[2,3-d]pyrimidine, 4-iodo-6-phenylis a chemical compound characterized by the molecular formula C11H7IN2S. It is a member of the thienopyrimidines class, featuring a thieno ring and a pyrimidine ring in its molecular structure. Thieno[2,3-d]pyrimidine, 4-iodo-6-phenylis distinguished by the presence of an iodine atom at the 4th position and a phenyl group at the 6th position. Its unique structural properties and reactivity suggest potential applications in pharmaceuticals or material science, although further research and testing are required to explore its full potential.
Uses
Used in Pharmaceutical Industry:
Thieno[2,3-d]pyrimidine, 4-iodo-6-phenylis used as a potential pharmaceutical agent for [application reason]. Its unique structure and reactivity may contribute to the development of new drugs or therapeutic agents, although further research is needed to fully understand its potential in this field.
Used in Material Science:
In the field of material science, Thieno[2,3-d]pyrimidine, 4-iodo-6-phenylis used as a potential material for [application reason]. Its structural properties may offer new opportunities for the development of advanced materials with specific properties, such as improved conductivity, stability, or other characteristics. Further investigation is necessary to determine its suitability and effectiveness in this context.
Check Digit Verification of cas no
The CAS Registry Mumber 718615-92-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,8,6,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 718615-92:
(8*7)+(7*1)+(6*8)+(5*6)+(4*1)+(3*5)+(2*9)+(1*2)=180
180 % 10 = 0
So 718615-92-0 is a valid CAS Registry Number.
718615-92-0Relevant articles and documents
4-Metalated condensed pyrimidines: Their preparation and reaction with aldehydes under barbier-type conditions
Therkelsen, Frans D.,Rottlaender, Mario,Thorup, Niels,Pedersen, Erik Bjerregaard
, p. 1991 - 1994 (2007/10/03)
Equation presented. The organometallic intermediate obtained from halogen-metal exchanges of 4-iodo-6-phenylthieno[2,3-d]pyrimidine under Barbier-type conditions was reacted with aldehydes to form the corresponding alcohols in moderate yields. The reaction involving an organolithium intermediate proceeded only at low temperature, whereas the reaction involving a magnesium ate intermediate also proceeded at room temperature. A crystal structure confirms that the expected constitutional alcohol isomer is formed, where no migration has taken place. The conditions were also suitable for 9-benzyl-6-iodopurine.
