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CS-W001157 4
Total: USD 88.00

(E)-3-Methoxyacrylic acid

  • CAS No. 6214-29-5

  • Cat. No. CS-0201343
  • Molecule weight102.09
  • Purity≥97%
  • MDL No.None

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

(E)-3-Methoxyacrylic acid|CS-0201343

Structure of 6214-29-5

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General Information

  • CAS No. 6214-29-5
  • Cat. No. CS-0201343
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄H₆O₃
  • Molecular Weight 102.09
  • Synonym(s) 3t-Methoxy-acrylsaeure
  • SMILES O=C(O)/C=C/OC

Description

(E)-3-Methoxyacrylic acid is a sterically constrained, electron-deficient enoate featuring a methoxy group at the β-position. This configuration enables direct participation in conjugate additions and Diels-Alder reactions under mild conditions. The compound exhibits enhanced stability compared to its α,β-unsaturated analogs, facilitating handling in synthetic workflows involving nucleophilic attack or polymerization initiation.

Application

(E)-3-Methoxyacrylic acid serves as a versatile building block for conjugated systems, enabling efficient access to α,β-unsaturated esters and amides via standard coupling reactions. Its stabilized enolate character facilitates Michael additions and Diels-Alder cycloadditions, while the methoxy group enhances solubility and offers a handle for further derivatization. Bench-stable and readily purified by recrystallization, it functions reliably in synthetic sequences requiring controlled reactivity and functional group compatibility.

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-P280-P302+P352

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Computational Chemistry Data

  • TPSA   46.53
  • LogP   0.2311
  • H_Acceptors   2
  • H_Donors   1
  • Rotatable_Bonds   2

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