581065-57-8 Usage
Uses
Used in Organic Synthesis:
TBG-13 is used as a building block in organic synthesis for its ability to form carbon-carbon bonds through Suzuki coupling reactions under mild conditions, making it a valuable reagent in this field.
Used in Pharmaceutical Research:
In pharmaceutical research, TBG-13 is utilized as a potential ligand in metal-catalyzed cross-coupling reactions, which can lead to the development of new and improved pharmaceutical compounds.
Used in Material Science:
TBG-13 has been studied for its application in the construction of functional polymers and materials, where its unique chemical structure and properties contribute to the development of advanced materials with specific characteristics.
Used in Cross-Coupling Reactions:
TBG-13 is used as a ligand in metal-catalyzed cross-coupling reactions, which are essential for the synthesis of complex organic molecules and have significant implications in the fields of chemistry and materials science.
Overall, TBG-13 is a versatile and valuable chemical with a wide range of potential applications in synthetic chemistry, material science, and pharmaceutical research.
Check Digit Verification of cas no
The CAS Registry Mumber 581065-57-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,8,1,0,6 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 581065-57:
(8*5)+(7*8)+(6*1)+(5*0)+(4*6)+(3*5)+(2*5)+(1*7)=158
158 % 10 = 8
So 581065-57-8 is a valid CAS Registry Number.
581065-57-8Relevant academic research and scientific papers
Synthesis of constrained raloxifene analogues by complementary use of Friedel-Crafts and directed remote metalation reactions
Kalinin, Alexey V.,Reed, Mark A.,Norman, Bryan H.,Snieckus, Victor
, p. 5992 - 5999 (2007/10/03)
New constrained heterocyclic analogues, 2a,b and 3, of Raloxifene (1) have been prepared by complementary Directed remote Metalation (DreM)/Friedel-Crafts cyclization approaches. Utilization of a benzylidene-thiolactone rearrangement was successfully impl
