Date published: 2026-2-10

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N-Boc-piperidine-4-boronic acid pinacol ester (CAS 1048970-17-7)

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Alternate Names:
1-Boc-piperidine-4-boronic acid pinacol ester; tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-piperidine-1-carboxylate
CAS Number:
1048970-17-7
Molecular Weight:
311.22
Molecular Formula:
C16H30BNO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-Boc-piperidine-4-boronic acid pinacol ester is a compound of interest in organic chemistry, particularly in the field of Suzuki coupling reactions, which are pivotal for creating carbon-carbon bonds in the synthesis of complex organic molecules. This compound, with its protected amino group and boronic acid moiety, provides a stable and reactive partner in cross-coupling processes, allowing researchers to construct a wide array of biologically active compounds and polymers with precise architectures. The piperidine ring, a common motif in many natural products and active compounds, is a point of focus for researchers exploring the conformational influences of cyclic structures on the efficacy of catalytic systems. In the study of molecular recognition and the design of selective receptors, the N-Boc-piperidine-4-boronic acid pinacol ester′s boronic ester function is employed due to its affinity for diol-containing molecules, which is for the advancement of sensing materials. Additionally, this compound is used in material science to investigate the creation of novel surface coatings and adhesives, where the boronate ester forms a key component for improving adhesion properties and chemical resistance.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Boc-piperidine-4-boronic acid pinacol ester, 1 g

sc-263821
1 g
$189.00

N-Boc-piperidine-4-boronic acid pinacol ester, 5 g

sc-263821A
5 g
$739.00