884507-45-3 Usage
Uses
Used in Pharmaceutical Industry:
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]pyrrolidine is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the formation of new carbon-carbon bonds through cross-coupling reactions. This enhances the development of complex molecular structures necessary for novel drug discovery.
Used in Agrochemical Industry:
In the agrochemical sector, 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]pyrrolidine is utilized as a reagent in the synthesis of agrochemicals, contributing to the creation of new compounds with potential applications in pest control and crop protection.
Used in Materials Science:
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]pyrrolidine is employed as a component in the development of advanced materials, leveraging its reactivity in cross-coupling reactions to produce materials with tailored properties for specific applications.
Used in Organic Synthesis:
As a reagent in organic synthesis, 1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]pyrrolidine is used for the synthesis of complex organic molecules, taking advantage of its boron-containing group to form new carbon-carbon bonds efficiently.
Used in Drug Development:
1-[3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl]pyrrolidine is studied for its potential in the development of new drugs, given its role in creating biologically active compounds through cross-coupling reactions, which is essential for medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 884507-45-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,4,5,0 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 884507-45:
(8*8)+(7*8)+(6*4)+(5*5)+(4*0)+(3*7)+(2*4)+(1*5)=203
203 % 10 = 3
So 884507-45-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H26BNO2/c1-16(2)17(3,4)21-18(20-16)15-9-7-8-14(12-15)13-19-10-5-6-11-19/h7-9,12H,5-6,10-11,13H2,1-4H3
884507-45-3Relevant academic research and scientific papers
AMPK INHIBITORS
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Page/Page column 49, (2019/06/17)
The 5'-AMP-activated protein kinase AMPK functions as a master switch to maintain cellular and whole-body energy homeostasis and abnormal activity profiles of AMPK may cause pathological disorders. The present invention relates to a series of compounds (I
Synthesis of amines with pendant boronic esters by borrowing hydrogen catalysis
Ma, Winson M. J.,James, Tony D.,Williams, Jonathan M. J.
, p. 4850 - 4853 (2013/10/08)
Amine alkylation reactions of alcohols have been performed in the presence of boronic ester groups to provide products which are known to have use as molecular sensors. The boronic ester moiety could be present in either the alcohol or amine starting mate
