(R)-Methyl 2-amino-3-(methylthio)propanoate hydrochloride

Name: (R)-Methyl 2-amino-3-(methylthio)propanoate hydrochloride
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CAS No. 34017-27-1
Cat. No. CS-0654810
Purity≥97%
MDL No.MFCD07438031

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(R)-Methyl 2-amino-3-(methylthio)propanoate hydrochloride|CS-0654810

Structure of 34017-27-1

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General Information

CAS No. 34017-27-1
Cat. No. CS-0654810
Purity ≥97%
MDL No. MFCD07438031
Storage RT, stored under nitrogen
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₅H₁₂ClNO₂S
Molecular Weight 185.67
Synonym(s) None
SMILES COC(=O)[C@H](CSC)N.Cl

Description

(R)-Methyl 2-amino-3-(methylthio)propanoate hydrochloride is a chiral building block featuring a stereodefined amino group and a sulfide-containing side chain. This bench-stable salt facilitates efficient incorporation into peptide architectures and complex heterocycles, offering predictable stereochemical outcomes in synthetic transformations.

Application

(R)-Methyl 2-amino-3-(methylthio)propanoate hydrochloride serves as a chiral building block for the synthesis of bioactive sulfonamides and peptidomimetics. The methylthio group provides orthogonal handle for selective transformations, while the protected amine and ester functionalities enable straightforward derivatization. Bench-stable and readily purified by recrystallization, it functions effectively in standard coupling and cyclization protocols.

Safety Information

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GHS Pictogram : N/A	GHS No : N/A
Signal Word : N/A	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : N/A
Precautionary Statements : N/A

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Computational Chemistry Data

TPSA 52.32
LogP 0.2715
H_Acceptors 4
H_Donors 1
Rotatable_Bonds 3

Other Classifications

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Fatty chain compounds

Life Science Amino Acids and their Derivatives Cysteine and derivatives

Chemical Biology Peptide Chemistry Unnatural Amino Acid Derivatives

Key Words

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(R)-Methyl 2-amino-3-(methylthio)propanoate hydrochloride

CAS No. 34017-27-1

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