272-24-2 Usage
Uses
Used in Pharmaceutical Research:
Thieno[2,3-d]pyrimidine (8CI,9CI) is used as a key building block for the synthesis of new compounds with various desirable properties. Its versatile structure allows for the development of molecules with potential anti-inflammatory, anti-cancer, and other biological activities, contributing to the advancement of drug discovery.
Used in Chemical Research:
In the field of chemical research, Thieno[2,3-d]pyrimidine (8CI,9CI) serves as a valuable component in the exploration of novel chemical reactions and the synthesis of complex organic molecules. Its unique fused ring system provides a platform for studying the properties and reactivity of heterocyclic compounds, further expanding the understanding of chemical synthesis and compound design.
Check Digit Verification of cas no
The CAS Registry Mumber 272-24-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 272-24:
(5*2)+(4*7)+(3*2)+(2*2)+(1*4)=52
52 % 10 = 2
So 272-24-2 is a valid CAS Registry Number.
272-24-2Relevant academic research and scientific papers
Rapid Access to Kinase Inhibitor Pharmacophores by Regioselective C-H Arylation of Thieno[2,3-d]pyrimidine
Flesch, Kaylin Nicole,Itami, Kenichiro,Murakami, Kei,Yamada, Shuya
supporting information, p. 1547 - 1551 (2020/03/13)
Regioselective C-H arylations of thieno[2,3-d]pyrimidine are accomplished under palladium catalysis. Thieno[2,3-d]pyrimidines react with aryl iodides at the C6-position and with aryl boronic acids at the C5-position, showing excellent regioselectivity. Me
CONDENSED HETEROAROMATIC RING SYSTEMS. VII. SYNTHESIS OF THIENOPYRIDINES, THIENOPYRIMIDINES, AND FUROPYRIDINES FROM o-SUBSTITUTED N-HETEROARYLACETYLENES
Sakamoto, Takao,Kondo, Yoshinori,Watanabe, Ryo,Yamanaka, Hiroshi
, p. 2719 - 2724 (2007/10/02)
The cross-coupling reaction of 2-chloro-3-iodo- and 4-chloro-3iodopyridines with phenylacetylene in the presence of dichlorobis(triphenylphosphine)palladium occured at the 3-position.The 3-ethynylpyridines containing an adjacent chloro group were converti
