832697-40-2 Usage
Uses
Used in Organic Synthesis:
1-N-BOC-PYRROLE-3-BORONIC ACID is used as a key intermediate for the synthesis of complex organic molecules, particularly in the pharmaceutical and chemical industries, due to its reactivity in cross-coupling reactions that facilitate the formation of carbon-carbon bonds.
Used in Pharmaceutical Research and Development:
In the pharmaceutical industry, 1-N-BOC-PYRROLE-3-BORONIC ACID is utilized as a building block for the development of new drugs, leveraging its ability to form stable intermediates and participate in various synthetic pathways that lead to the creation of bioactive compounds.
Used in Chemical Manufacturing:
1-N-BOC-PYRROLE-3-BORONIC ACID is employed as a reagent in the manufacturing of specialty chemicals, where its unique chemical properties allow for the production of compounds with specific functionalities and applications in various fields, such as materials science and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 832697-40-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,3,2,6,9 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 832697-40:
(8*8)+(7*3)+(6*2)+(5*6)+(4*9)+(3*7)+(2*4)+(1*0)=192
192 % 10 = 2
So 832697-40-2 is a valid CAS Registry Number.
832697-40-2Relevant academic research and scientific papers
Development of a Br?nsted acid-promoted arene-ynamide cyclization toward the total syntheses of marinoquinolines A and C and aplidiopsamine A
Yamaoka, Yousuke,Yoshida, Takahiro,Shinozaki, Makiko,Yamada, Ken-Ichi,Takasu, Kiyosei
, p. 957 - 964 (2015/03/05)
(Chemical Equation Presented) A Br?nsted acid-promoted arene-ynamide cyclization has been developed to construct the 3H-pyrrolo[2,3-c]quinolines. This reaction consists of the generation of a highly reactive keteniminium intermediate from arene-ynamide activated by a Br?nsted acid and electrophilic aromatic substitution reaction to give arene-fused quinolines in high yields. This methodology enabled facile access to marinoquinolines A and C and aplidiopsamine A.
