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CS-W001157 4
Total: USD 88.00

3-Acrylamidobenzoic acid

  • CAS No. 17090-28-7

  • Cat. No. CS-0132533
  • Purity≥98%
  • MDL No.None

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

3-Acrylamidobenzoic acid|CS-0132533

Structure of 17090-28-7

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General Information

  • CAS No. 17090-28-7
  • Cat. No. CS-0132533
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₉NO₃
  • Molecular Weight 191.18
  • Synonym(s) 3-(prop-2-enoylamino)benzoic acid
  • SMILES O=C(O)C1=CC=CC(NC(C=C)=O)=C1

Description

3-Acrylamidobenzoic acid integrates a reactive acrylamide group with a carboxylic acid functionality, enabling efficient conjugation to biomolecules via amine coupling. The para-positioned carboxylate enhances solubility and facilitates derivatization in aqueous media. This bifunctional architecture supports robust bioconjugation under mild conditions.

Application

3-Acrylamidobenzoic acid serves as a versatile building block for conjugate addition reactions and polymerizable scaffolds. Its acrylamide functionality enables efficient Michael additions, while the carboxylic acid group facilitates coupling reactions and derivatization. The molecule exhibits good bench stability and is compatible with standard functional group transformations, making it well-suited for applications in bioconjugation, materials science, and heterocycle 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

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Computational Chemistry Data

  • TPSA   66.4
  • LogP   1.5093
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   3

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