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CS-W001157 4
Total: USD 88.00

(E)-Oct-2-enoic acid

  • CAS No. 1871-67-6

  • Cat. No. CS-0098436
  • Purity≥98%
  • MDL No.MFCD00002706

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

(E)-Oct-2-enoic acid|CS-0098436

Structure of 1871-67-6

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General Information

  • CAS No. 1871-67-6
  • Cat. No. CS-0098436
  • Purity ≥98%
  • MDL No. MFCD00002706
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₁₄O₂
  • Molecular Weight 142.20
  • Synonym(s) None
  • SMILES CCCCC/C=C/C(O)=O

Description

(E)-Oct-2-enoic acid features a conjugated enoic system with defined (E)-stereochemistry, enabling precise incorporation into lipid-based scaffolds and functional materials. This bench-stable, moisture-tolerant reagent delivers high regioselectivity in coupling reactions and serves as a key building block for bioactive esters and polymer precursors under standard conditions.

Application

(E)-Oct-2-enoic acid serves as a versatile building block for conjugated unsaturated systems, enabling efficient Michael additions and Diels-Alder reactions. Its stable (E)-configuration facilitates reproducible stereocontrol in synthetic sequences, while the carboxylic acid functionality allows direct derivatization or activation for amide bond formation. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for use in medicinal chemistry and materials synthesis workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS05
Signal Word : Danger
UN#: 3265
Class : 8
Packing Group : Ⅱ
Hazard Statements : H314
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501

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Computational Chemistry Data

  • TPSA   37.3
  • LogP   2.2075
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   5

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