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tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate

  • CAS No. 1048970-17-7

  • Cat. No. CS-W009011
  • Purity≥95%
  • MDL No.MFCD09997792

*For research and further manufacturing use only, not for direct human use.

tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate|CS-W009011

Structure of 1048970-17-7

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General Information

  • CAS No. 1048970-17-7
  • Cat. No. CS-W009011
  • Purity ≥95%
  • MDL No. MFCD09997792
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₆H₃₀BNO₄
  • Molecular Weight 311.22
  • Synonym(s) Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidin-1-carboxylate
  • SMILES O=C(OC(C)(C)C)N1CCC(CC1)B(OC(C)2C)OC2(C)C

Description

tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)piperidine-1-carboxylate is a bench-stable boronate building block featuring a piperidine core with a sterically protected boronate ester. This derivative enables efficient cross-coupling reactions under mild conditions, integrating seamlessly into complex molecular architectures. The tetramethyl-substituted dioxaborolane enhances stability and functional group tolerance during synthetic workflows.

Synthesis

  • Route1

    References

    • INFINITY PHARMACEUTICALS, INC.; CASTRO, Alfredo, C.; EVANS, Catherine, A.; GRENIER, Louis; GROGAN, Michael, J. Patent: WO2010/118159 A1, 2010 ; Location in patent: Page/Page column 64-65; 67-68 ;
  • Route2

    References

    • Yang, Chu-Ting; Zhang, Zhen-Qi; Tajuddin, Hazmi; Wu, Chen-Cheng; Liang, Jun; Liu, Jing-Hui; Fu, Yao; Czyzewska, Maria; Steel, Patrick G.; Marder, Todd B.; Liu, Lei Angewandte Chemie - International Edition, 2012 , vol. 51, # 2 p. 528 - 532

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   48
  • LogP   3.4797
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   1

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