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CS-W001157 4
Total: USD 88.00

Boc-C9-COOH

  • CAS No. 1789702-17-5

  • Cat. No. CS-0162544
  • Purity≥97%
  • MDL No.MFCD30737824

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

Boc-C9-COOH|CS-0162544

Structure of 1789702-17-5

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General Information

  • CAS No. 1789702-17-5
  • Cat. No. CS-0162544
  • Purity ≥97%
  • MDL No. MFCD30737824
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₅H₂₈O₄
  • Molecular Weight 272.39
  • Synonym(s) None
  • SMILES O=C(O)CCCCCCCCCC(=O)OC(C)(C)C

Description

11-(tert-Butoxy)-11-oxoundecanoic acid features a sterically hindered tert-butoxy group flanking a ketone and carboxylic acid functionalization, enabling selective derivatization in complex synthetic sequences. This bench-stable scaffold facilitates the construction of advanced intermediates for medicinal chemistry and macrocyclic compound synthesis under standard conditions.

Application

11-(tert-Butoxy)-11-oxoundecanoic acid serves as a versatile building block for the synthesis of γ-keto esters and lactones, enabling efficient access to bioactive heterocyclic scaffolds. Its tert-butoxy carbonyl group provides excellent stability and orthogonal reactivity, facilitating selective transformations in complex molecule assembly. The molecule's α,β-unsaturated ketone functionality supports diverse conjugate additions and cyclization reactions, making it valuable in medicinal chemistry and natural product synthesis 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 : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

Quality Control

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Computational Chemistry Data

  • TPSA   63.6
  • LogP   3.9236
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   10

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