956378-39-5 Usage
Uses
Used in Organic Synthesis:
[4'-(but-3-en-1-yloxy)biphenyl-4-yl]boronic acid is used as a building block in organic synthesis for the creation of complex molecules and materials. Its unique reactivity allows it to participate in various chemical reactions, making it a valuable component in the synthesis process.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, [4'-(but-3-en-1-yloxy)biphenyl-4-yl]boronic acid is used as a key intermediate for the development of pharmaceuticals. Its unique structure and reactivity enable the synthesis of novel drug candidates with potential therapeutic applications.
Used in Materials Science:
[4'-(but-3-en-1-yloxy)biphenyl-4-yl]boronic acid is also utilized in materials science as a component in the design and synthesis of advanced materials with specific properties. Its incorporation into these materials can lead to enhanced performance characteristics, such as improved mechanical strength, thermal stability, or electrical conductivity.
Used in Suzuki-Miyaura Cross-Coupling:
This chemical compound is used as a reactant in Suzuki-Miyaura cross-coupling reactions, a widely employed method in organic chemistry for the formation of carbon-carbon bonds. Its participation in these reactions allows for the efficient synthesis of a variety of organic molecules, including those with potential applications in the pharmaceutical and chemical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 956378-39-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,3,7 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 956378-39:
(8*9)+(7*5)+(6*6)+(5*3)+(4*7)+(3*8)+(2*3)+(1*9)=225
225 % 10 = 5
So 956378-39-5 is a valid CAS Registry Number.
956378-39-5Relevant academic research and scientific papers
Nontemplated versus templated synthesis of a 56-membered macrocycle
Albrecht, Markus,Yeni,Fr?hlich, Roland
, p. 2295 - 2297 (2008/02/09)
The amine-substituted quinquephenylene 1 was prepared in a Suzuki coupling approach and by reaction with terephthalic dialdehyde (7) it was transformed into the phenyl-connected diimine 8. Ring-closing metathesis with the Grubbs I or II catalyst led to the corresponding macrocycle 9. Hydrogenation resulted in the reduction of the double bonds as well as the removal of the template to yield the 56-membered macrocycle 6 in an overall yield of 43% (from 1). Direct metathesis reaction of 1 followed by hydrogenation afforded 6 in only 21% yield. Georg Thieme Verlag Stuttgart.
