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CS-W001157 4
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Ethyl 3-Amino-4-hydroxybenzoate

  • CAS No. 13052-92-1

  • Cat. No. CS-0040877
  • Purity≥97%
  • MDL No.MFCD09961411

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

Ethyl 3-Amino-4-hydroxybenzoate|CS-0040877

Structure of 13052-92-1

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General Information

  • CAS No. 13052-92-1
  • Cat. No. CS-0040877
  • Purity ≥97%
  • MDL No. MFCD09961411
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₁NO₃
  • Molecular Weight 181.19
  • Synonym(s) Benzoic acid, 3-amino-4-hydroxy-, ethyl ester
  • SMILES O=C(OCC)C1=CC=C(O)C(N)=C1

Description

Ethyl 3-amino-4-hydroxybenzoate features a dual functional handle—amine and phenolic hydroxyl—enabling versatile conjugation and derivatization. This bench-stable, moisture-tolerant compound integrates readily into bioconjugation workflows and serves as a key intermediate in the synthesis of pharmaceutical analogs and fluorescent probes.

Application

Ethyl 3-amino-4-hydroxybenzoate serves as a versatile building block in medicinal chemistry, enabling direct access to hydroxylated and amino-substituted benzene scaffolds. The molecule’s dual functional groups—phenolic hydroxyl and primary amine—facilitate sequential derivatization, including acylation, alkylation, and coupling reactions. Its bench-stable nature and compatibility with standard purification methods make it well-suited for use in multi-step synthesis of heterocyclic intermediates and API precursors.

Safety Information

Download SDS
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

Quality Control

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Computational Chemistry Data

  • TPSA   72.55
  • LogP   1.1511
  • H_Acceptors   4
  • H_Donors   2
  • Rotatable_Bonds   2

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