161282-93-5 Usage
Description
(E)-(2-Cyclopentylethenyl)boronic Acid is an organic compound featuring a cyclopentane ring with a vinyl group and a boronic acid functional group. It is a white solid and is known for its reactivity in various chemical reactions, particularly in the field of organic synthesis.
Uses
Used in Chemical Synthesis:
(E)-(2-Cyclopentylethenyl)boronic Acid is used as a reagent in the Suzuki-Miyaura cross-coupling reaction for the formation of carbon-carbon bonds. This reaction is a powerful tool in organic chemistry, allowing the creation of complex molecular structures and the synthesis of various compounds, including pharmaceuticals, agrochemicals, and advanced materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (E)-(2-Cyclopentylethenyl)boronic Acid is used as a key intermediate in the synthesis of various drug molecules. Its ability to form carbon-carbon bonds through the Suzuki-Miyaura cross-coupling reaction makes it a valuable component in the development of new medications with improved efficacy and reduced side effects.
Used in Material Science:
(E)-(2-Cyclopentylethenyl)boronic Acid is also utilized in the field of material science for the synthesis of advanced materials with specific properties. These materials can be used in various applications, such as electronics, energy storage, and coatings, where their unique characteristics can provide enhanced performance and functionality.
Check Digit Verification of cas no
The CAS Registry Mumber 161282-93-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,2,8 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 161282-93:
(8*1)+(7*6)+(6*1)+(5*2)+(4*8)+(3*2)+(2*9)+(1*3)=125
125 % 10 = 5
So 161282-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H13BO2/c9-8(10)6-5-7-3-1-2-4-7/h5-7,9-10H,1-4H2/b6-5+
161282-93-5Relevant articles and documents
Palladium catalysed tandem cyclisation-anion capture. Part 8: Cascade hydrostannylation-cyclisation-anion capture and cascade hydroboration-cyclisation-anion capture on solid phase
Grigg, Ronald,MacLachlan, William S,MacPherson, David T,Sridharan, Visuvanathar,Suganthan, Selvaratnam
, p. 10335 - 10345 (2007/10/03)
Up to four bonds and five stereocentres are created, in five component processes (five point diversity), utilising resin bound aryl iodides by hydroboration or hydrostannylation of alkynes, followed by cyclisation-anion capture involving Suzuki or Stille reactions. Three small libraries were prepared to validate the chemistry.
