1278579-62-6 Usage
Chemical structure
The compound consists of a piperidine ring attached to a thiophene ring, with a boron-containing group (tetramethyl-1,3,2-dioxaborolan-2-yl) as a substituent.
Boron-containing group
The specific boron-containing group is a tetramethyl-1,3,2-dioxaborolan-2-yl group, which is known for its stability and reactivity in organic synthesis.
Potential applications
The compound has potential applications in the field of organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds.
Medicinal chemistry
It may also have uses in medicinal chemistry, as the unique structure of the compound could be exploited for the development of new drugs or drug candidates.
Building block
The compound can serve as a building block for various functional materials, due to its versatile chemical structure and the presence of the boron-containing group.
Further investigation
The specific properties and potential uses of 1-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl)piperidine would need to be further investigated through research and experimentation to fully understand its capabilities and limitations.
Stability
The presence of the tetramethyl-1,3,2-dioxaborolan-2-yl group suggests that the compound may have good stability, which is important for its use in various applications.
Reactivity
The boron-containing group is known for its reactivity in organic synthesis, which could make the compound a useful intermediate or building block in the synthesis of more complex molecules.
Heteroatom bonding
The presence of both nitrogen (from the piperidine ring) and sulfur (from the thiophene ring) in the compound suggests that it may be capable of forming carbon-heteroatom bonds, which are important in the synthesis of various organic compounds.
Structural diversity
The combination of the piperidine and thiophene rings, along with the boron-containing group, provides a unique structural diversity that could be exploited in the design of new molecules and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1278579-62-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,7,8,5,7 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1278579-62:
(9*1)+(8*2)+(7*7)+(6*8)+(5*5)+(4*7)+(3*9)+(2*6)+(1*2)=216
216 % 10 = 6
So 1278579-62-6 is a valid CAS Registry Number.
1278579-62-6Relevant articles and documents
Live cell cytoplasm staining and selective labeling of intracellular proteins by non-toxic cell-permeant thiophene fluorophores
Di Maria,Palama,Baroncini,Barbieri,Bongini,Bizzarri,Gigli,Barbarella
supporting information, p. 1603 - 1610 (2014/03/21)
A structurally correlated series of cell-permeant thiophene fluorophores, characterized by intense green or red fluorescence inside live mouse embryonic fibroblasts, was developed. The fluorophores displayed rapid internalization, excellent retention inside the cells, and high optical stability in the cytosolic environment and did not alter cell viability and reproducibility. Depending on the molecular structure, they experienced distinct fate inside the cells: from bright and lasting staining of the cytoplasm to selective tagging of a small set of globular proteins. This journal is The Royal Society of Chemistry 2014.
PROCESS FOR THE BORYLATION OF ARENES AND HETEROARYLS
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Page/Page column 44, (2012/03/26)
This invention relates to a novel process for the borylation of arenes and heteroaryls. The present invention also provides novel borenium cations, which act as electrophiles for electrophilic substitution on the arene or heteroaryl ring, as well as to methodology for the preparation of these cations.
