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tert-Butyl (1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate

  • CAS No. 1004294-78-3

  • Cat. No. CS-0162403
  • Purity≥96%
  • MDL No.None

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

tert-Butyl (1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate|CS-0162403

Structure of 1004294-78-3

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General Information

  • CAS No. 1004294-78-3
  • Cat. No. CS-0162403
  • Purity ≥96%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₀H₃₀BNO₄
  • Molecular Weight 359.27
  • Synonym(s) Carbamic acid, N-[1-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclopropyl]-, 1,1-dimethylethyl ester
  • SMILES O=C(OC(C)(C)C)NC1(C2=CC=CC(B3OC(C)(C)C(C)(C)O3)=C2)CC1

Description

tert-Butyl (1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate features a boronate ester group integrated with a cyclopropyl scaffold, enabling robust Suzuki-Miyaura coupling reactions. The tetramethyl-substituted dioxaborolane moiety enhances stability and reactivity under standard conditions. This bench-stable reagent simplifies the construction of complex arylated architectures in medicinal chemistry and materials synthesis.

Application

tert-Butyl (1-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropyl)carbamate serves as a robust boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The cyclopropyl scaffold imparts structural rigidity and metabolic stability, while the Bpin group enables efficient coupling under mild conditions. Its tert-butyl carbamate protecting group ensures excellent bench stability, ease of purification, and compatibility with diverse functional groups, making it ideal for constructing complex pharmaceutical intermediates and heterocyclic scaffolds in medicinal chemistry workflows.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   56.79
  • LogP   3.4996
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   3

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