163079-25-2 Usage
Uses
Used in Chemical Synthesis:
2-(tert-Butyldimethylsilyl)thiophene is used as a key intermediate in the synthesis of various complex organic molecules. Its presence in the molecule allows for the formation of stable intermediates that can be further modified or functionalized, facilitating the creation of a wide range of chemical compounds.
Used in Pharmaceutical Manufacturing:
2-(tert-Butyldimethylsilyl)thiophene is used as a building block in the development of new pharmaceutical compounds. Its ability to form stable and complex molecular structures makes it a valuable component in the synthesis of potential drug candidates, contributing to the advancement of novel therapeutic agents.
Used in Research and Development:
2-(tert-Butyldimethylsilyl)thiophene is used as a research tool in the study of chemical reactions and the development of new synthetic methodologies. Its unique reactivity and stability make it an ideal candidate for exploring new reaction pathways and understanding the underlying mechanisms of various chemical processes.
Used in Material Science:
2-(tert-Butyldimethylsilyl)thiophene is used as a component in the development of new materials with specific properties, such as high thermal stability or hydrophobicity. Its incorporation into the molecular structure of these materials can lead to the creation of innovative products with applications in various industries, including electronics, coatings, and textiles.
Check Digit Verification of cas no
The CAS Registry Mumber 163079-25-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,0,7 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 163079-25:
(8*1)+(7*6)+(6*3)+(5*0)+(4*7)+(3*9)+(2*2)+(1*5)=132
132 % 10 = 2
So 163079-25-2 is a valid CAS Registry Number.
163079-25-2Relevant academic research and scientific papers
Synthetic Applications of Arenetricarbonylchromium(0) Complexes: the Synthesis of Polyfunctionalised Thiophenes
Loft, Michael S.,Mowlem, Timothy J.,Widdowson, David A.
, p. 97 - 104 (2007/10/02)
Lithiation of thiophenetricarbonylchromium(0) complexes with butyllithium occurs preferentially at C-2/5 but when these are blocked, 3/4 lithiation is facile.Combinations of a bulky silyl (i-Pr3Si or t-BuMe2Si) blocking group at C-2/5 and remote lithiation/electrophilic quench of C-3/4 followed by desilylation/lithiation/electrophilic quench allowed the synthesis of 2,3-, 2,3,5- and 2,3,4,5-polysubstituted thiophene complexes and their derived free thiophenes.
