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Methyl (R)-2-aminobutanoate hydrochloride

  • CAS No. 85774-09-0

  • Cat. No. CS-0059300
  • Molecule weight153.61
  • Purity≥96%
  • MDL No.MFCD10565758

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

Methyl (R)-2-aminobutanoate hydrochloride|CS-0059300

Structure of 85774-09-0

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General Information

  • CAS No. 85774-09-0
  • Cat. No. CS-0059300
  • Purity ≥96%
  • MDL No. MFCD10565758
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₁₂ClNO₂
  • Molecular Weight 153.61
  • Synonym(s) methyl (2R)-2-aminobutanoate hydrochloride
  • SMILES [H]Cl.CC[C@@H](N)C(OC)=O

Description

Methyl (R)-2-aminobutanoate hydrochloride is a chiral building block featuring a stereodefined amino group and a methyl ester functionality. This bench-stable derivative enables direct incorporation into peptide synthesis and asymmetric catalysis, offering high reactivity under standard conditions with minimal racemization.

Application

Methyl (R)-2-aminobutanoate hydrochloride serves as a chiral building block for synthesizing bioactive molecules, particularly in the development of pharmaceutical intermediates. Its well-defined stereochemistry enables stereoselective transformations, while the protected amine and ester functionalities offer orthogonal reactivity. The hydrochloride salt enhances bench stability and simplifies handling, facilitating purification and integration into standard peptide coupling and asymmetric synthesis workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   52.32
  • LogP   0.3185
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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