115545-85-2 | Methyl (2S)-2-amino-3-[(triphenylmethyl)sulfanyl]propanoate

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$49.00	$34.00
1g	95%	in stock	$136.00	$95.00
5g	95%	in stock	$518.00	$363.00

Description

• Catalog Number: AI09822
• Chemical Name: Methyl (2S)-2-amino-3-[(triphenylmethyl)sulfanyl]propanoate
• CAS Number: 115545-85-2
• Molecular Formula: C23H23NO2S
• Molecular Weight: 377.4992
• MDL Number: MFCD27578273
• SMILES: COC(=O)[C@@H](CSC(c1ccccc1)(c1ccccc1)c1ccccc1)N

Computed Properties

• Complexity: 406
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 27
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 8
• XLogP3: 4.6

Upstream Synthesis Route

(S)-Methyl 2-amino-3-(tritylthio)propanoate - an essential reagent in organic synthesis. This compound plays a key role in the preparation of various important molecules through chemical reactions. It is commonly used as a chiral building block in the synthesis of biologically active compounds, pharmaceutical agents, and complex organic molecules.One significant application of (S)-Methyl 2-amino-3-(tritylthio)propanoate is in the asymmetric synthesis of amino acids. By utilizing this compound, chemists can introduce chirality into molecular structures, enabling the selective formation of enantiomerically pure amino acids. This capability is crucial in the development of pharmaceuticals, where the stereochemistry of molecules can greatly influence their biological activity.Moreover, (S)-Methyl 2-amino-3-(tritylthio)propanoate is valuable in peptide synthesis. Peptides are essential components in many biological processes and serve as targets for drug development. Using this compound in peptide coupling reactions allows for the controlled assembly of peptide chains with specific chirality, leading to the creation of peptide-based drugs, catalysts, and other bioactive molecules.In summary, (S)-Methyl 2-amino-3-(tritylthio)propanoate is a versatile and indispensable tool in chemical synthesis, enabling the creation of complex molecules with tailored chirality for various applications in medicinal chemistry, materials science, and biochemistry.