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(4-((4-((tert-butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid is an organoboronic acid that features a phenyl group, a boronic acid functional group, a piperidine ring, and a tert-butyldimethylsilyl (TBS) protecting group. This versatile chemical is used in the preparation of various organic compounds.
Used in Organic Synthesis:
(4-((4-((tert-butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid is used as a reagent for cross-coupling reactions and other transformations in organic synthesis. The boronic acid moiety allows it to act as a Lewis acid, forming coordination complexes with various substrates.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4-((4-((tert-butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid is used as a building block for the synthesis of complex organic molecules, including potential drug candidates. The TBS protecting group shields reactive functional groups from unwanted reactions during synthesis, ensuring the desired product is obtained.
Used in Material Science:
(4-((4-((tert-butyldimethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid is also used in material science for the development of new materials with specific properties. (4-((4-((tert-butyldiMethylsilyl)oxy)piperidin-1-yl)sulfonyl)phenyl)boronic acid's reactivity and selectivity, influenced by the piperidine ring, can be harnessed to create materials with tailored characteristics for various applications.

1704065-62-2

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1704065-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1704065-62-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,7,0,4,0,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1704065-62:
(9*1)+(8*7)+(7*0)+(6*4)+(5*0)+(4*6)+(3*5)+(2*6)+(1*2)=142
142 % 10 = 2
So 1704065-62-2 is a valid CAS Registry Number.

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