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CS-W001157 4
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Methyl (R)-4-(1-aminoethyl)benzoate hydrochloride

  • CAS No. 1097196-96-7

  • Cat. No. CS-0131595
  • Purity≥98%
  • MDL No.MFCD12910780

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

Methyl (R)-4-(1-aminoethyl)benzoate hydrochloride|CS-0131595

Structure of 1097196-96-7

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General Information

  • CAS No. 1097196-96-7
  • Cat. No. CS-0131595
  • Purity ≥98%
  • MDL No. MFCD12910780
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₀H₁₄ClNO₂
  • Molecular Weight 215.68
  • Synonym(s) (R)-4-(1-Amino-ethyl)-benzoic acid methyl ester hydrochloride
  • SMILES O=C(OC)C1=CC=C([C@H](N)C)C=C1.[H]Cl

Description

Methyl (R)-4-(1-aminoethyl)benzoate hydrochloride features a chiral α-aminoethyl side chain that enables stereoselective coupling in peptide synthesis. The benzoate ester group provides solubility and reactivity under standard conditions, while the hydrochloride salt enhances stability and handling. This compound serves as a key building block for bioactive molecule construction.

Application

Methyl (R)-4-(1-aminoethyl)benzoate hydrochloride serves as a chiral building block for the synthesis of bioactive compounds, enabling efficient access to substituted benzamides and amino acid derivatives. The protected amine and ester functionalities offer orthogonal reactivity, facilitating selective transformations in medicinal chemistry workflows. Bench-stable and readily purified by recrystallization, it functions effectively in standard coupling and reduction 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-P280-P302+P352

Quality Control

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Computational Chemistry Data

  • TPSA   52.32
  • LogP   1.9147
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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