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CS-W001157 4
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(R)-Methyl 2-amino-3-methoxypropanoate hydrochloride

  • CAS No. 1800300-79-1

  • Cat. No. CS-0162497
  • Purity≥97%
  • MDL No.None

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

(R)-Methyl 2-amino-3-methoxypropanoate hydrochloride|CS-0162497

Structure of 1800300-79-1

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General Information

  • CAS No. 1800300-79-1
  • Cat. No. CS-0162497
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₁₂ClNO₃
  • Molecular Weight 169.61
  • Synonym(s) D-Ser(me)-Ome.Hcl
  • SMILES O=C(OC)[C@H](N)COC.[H]Cl

Description

(R)-Methyl 2-amino-3-methoxypropanoate hydrochloride features a chiral α-amino acid scaffold with a methoxy group at the β-position, delivering enhanced solubility and stability under standard conditions. This bench-stable derivative integrates readily into peptide synthesis workflows, serving as a key building block for bioactive peptidomimetics and enzyme inhibitors.

Application

(R)-Methyl 2-amino-3-methoxypropanoate hydrochloride serves as a stereocontrolled building block for the synthesis of β-amino alcohols and peptidomimetics. Its chiral center enables stereoselective transformations, while the methoxy group enhances solubility and stability. The hydrochloride salt improves handling and crystallinity, facilitating purification and consistent performance in standard amine-functionalization reactions.

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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   61.55
  • LogP   -0.4451
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   3

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