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CS-W001157 4
Total: USD 88.00

(R)-4-(1-aminoethyl)benzoic acid

  • CAS No. 1108683-66-4

  • Cat. No. CS-D0716
  • Purity≥95%
  • MDL No.MFCD06761798

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

(R)-4-(1-aminoethyl)benzoic acid|CS-D0716

Structure of 1108683-66-4

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General Information

  • CAS No. 1108683-66-4
  • Cat. No. CS-D0716
  • Purity ≥95%
  • MDL No. MFCD06761798
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₁NO₂
  • Molecular Weight 165.19
  • Synonym(s) None
  • SMILES O=C(O)C1=CC=C([C@@H](C)N)C=C1

Description

(R)-4-(1-Aminoethyl)benzoic acid features a chiral α-amino group adjacent to a para-substituted aromatic ring, delivering a rigid, electron-rich scaffold for asymmetric synthesis. This bench-stable derivative integrates seamlessly into peptide-like architectures and serves as a key intermediate in the development of bioactive molecules requiring defined stereochemistry.

Application

(R)-4-(1-Aminoethyl)benzoic acid serves as a chiral building block for bioactive molecules, enabling stereoselective synthesis of pharmaceutical intermediates. Its carboxylic acid and primary amine functionalities offer orthogonal reactivity for peptide coupling and conjugation strategies. The stable (R)-configuration facilitates reproducible asymmetric synthesis, while the benzoic acid core supports derivatization via standard electrophilic aromatic substitution and catalytic hydrogenation protocols.

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   63.32
  • LogP   1.4045
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   2

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