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CS-W001157 4
Total: USD 88.00

(E)-Methyl 3-(3-aminophenyl)acrylate

  • CAS No. 163487-10-3

  • Cat. No. CS-0036729
  • Purity≥97%
  • MDL No.None

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

(E)-Methyl 3-(3-aminophenyl)acrylate|CS-0036729

Structure of 163487-10-3

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General Information

  • CAS No. 163487-10-3
  • Cat. No. CS-0036729
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₁NO₂
  • Molecular Weight 177.20
  • Synonym(s) methyl (E)-3-(3-aminophenyl)prop-2-enoate
  • SMILES COC(=O)/C=C/C1=CC(=CC=C1)N

Description

(E)-Methyl 3-(3-aminophenyl)acrylate features a conjugated acrylate system paired with a para-amino aromatic group, enabling efficient integration into diverse synthetic scaffolds. This electron-rich enone moiety facilitates nucleophilic additions and serves as a key building block in pharmaceutical and agrochemical synthesis. The methyl ester functionality supports further derivatization under standard conditions.

Application

(E)-Methyl 3-(3-aminophenyl)acrylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted anilines and heterocyclic scaffolds. The conjugated enamide system exhibits robust stability under standard bench conditions and tolerates diverse functional groups, facilitating downstream transformations such as Suzuki-Miyaura coupling, electrophilic substitution, and cyclization reactions. Its amine functionality provides a direct handle for derivatization, while the ester group supports selective reduction or hydrolysis—making it particularly valuable in medicinal chemistry lead optimization and API precursor synthesis.

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-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   52.32
  • LogP   1.455
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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