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65672-32-4

N-α-Methyl-L-alanine hydrochloride

Catalog#: AR00FGRM  |   CAS#: 65672-32-4  |   MDL#: MFCD00754492  |   MF: C4H10ClNO2  |   MW: 139.5807

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Catalog Number AR00FGRM
Chemical Name N-α-Methyl-L-alanine hydrochloride
CAS Number 65672-32-4
Molecular Formula C4H10ClNO2
Molecular Weight 139.5807
MDL Number MFCD00754492
SMILES C[C@@H](C(=O)O)NC.Cl

As a professional chemist, I can describe the application of H-N-Me-Ala-OH.HCl in chemical synthesis. This compound, H-N-Me-Ala-OH.HCl, is a type of protected amino acid derivative commonly used in peptide synthesis. Peptides are important molecules in biological and pharmaceutical research, as they play crucial roles in various physiological processes and can serve as potential therapeutic agents.In chemical synthesis, H-N-Me-Ala-OH.HCl serves as a building block for constructing peptides, particularly those containing alanine residues. The "H-N-Me-Ala" portion represents an N-methylated alanine residue, which is often incorporated into peptides to modulate their properties, such as stability and bioactivity.H-N-Me-Ala-OH.HCl is typically utilized in solid-phase peptide synthesis (SPPS), a widely used method for assembling peptides in a stepwise fashion on a solid support. In this process, the amino group of H-N-Me-Ala-OH.HCl is activated and coupled with the carboxylic acid group of the preceding amino acid, leading to the formation of peptide bonds. The HCl salt form of H-N-Me-Ala-OH helps in maintaining the stability and solubility of the compound during the synthesis reactions.Overall, H-N-Me-Ala-OH.HCl plays a crucial role in enabling the efficient and controlled synthesis of peptides with specific sequences and functionalities, making it a valuable tool in peptide chemistry and drug discovery efforts.
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GHS Pictogram N/A
UN# -
Hazard Statements -
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