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(R)-Methyl 3-aminobutanoate

  • CAS No. 103189-63-5

  • Cat. No. CS-0003933
  • Purity≥97%
  • MDL No.MFCD08058803

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

(R)-Methyl 3-aminobutanoate|CS-0003933

Structure of 103189-63-5

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General Information

  • CAS No. 103189-63-5
  • Cat. No. CS-0003933
  • Purity ≥97%
  • MDL No. MFCD08058803
  • Storage -20°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₁₁NO₂
  • Molecular Weight None
  • Synonym(s) Methyl (R)-3-Aminobutanoate
  • SMILES O=C(OC)C[C@@H](C)N

Description

(R)-Methyl 3-aminobutanoate is a chiral building block featuring a stereodefined (R)-configured alpha-amino acid derivative. This bench-stable, moisture-tolerant amine integrates readily into peptide synthesis and asymmetric catalysis. The methyl ester group enables selective derivatization, while the primary amine supports conjugation and functionalization in medicinal chemistry applications.

Application

(R)-Methyl 3-aminobutanoate serves as a chiral building block for the synthesis of bioactive molecules, enabling efficient access to (R)-configured amino acid derivatives. Its stability under standard reaction conditions and compatibility with common coupling protocols facilitate straightforward functionalization. The molecule functions as a key intermediate in the construction of heterocyclic scaffolds and peptidomimetics, offering predictable stereochemical control and ease of purification in scalable processes.

Safety Information

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GHS Pictogram :
GHS No : GHS02,GHS07
Signal Word : Danger
UN#: 3272
Class : 3
Packing Group : Ⅲ
Hazard Statements : H226-H315-H319-H335-H413
Precautionary Statements : P210-P240-P241-P280-P370+P378

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Computational Chemistry Data

  • TPSA   52.32
  • LogP   -0.1033
  • H_Acceptors   3
  • H_Donors   1
  • Rotatable_Bonds   2

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