S-Trityl-L-cysteine

• CAT Number: R004262
• CAS Number: 2799-07-7
• Molecular Formula: C22H21NO2S
• Molecular Weight: 363.47
• Purity: ≥95%
• Synonyms: S-(Triphenylmethyl)-L-cysteine; (2R)-2-Amino-3-[(triphenylmethyl)thio]propanoic Acid; 3-Tritylthio-L-alanine; NSC 83265; S-Triphenylmethyl-L-cysteine; S-Trityl-(R)-cysteine; S-Tritylcysteine; Tritylthioalanine
• Target: Cytoskeleton
• Storage: -20°C
• IUPAC Name: (2R)-2-amino-3-tritylsulfanylpropanoic acid
• InChI: InChI=1S/C22H21NO2S/c23-20(21(24)25)16-26-22(17-10-4-1-5-11-17,18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-15,20H,16,23H2,(H,24,25)/t20-/m0/s1
• InChIKey: DLMYFMLKORXJPO-FQEVSTJZSA-N
• SMILES: C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)SCC(C(=O)O)N

S-Trityl-L-cysteine(Cat No.:R004262) is a chemical compound utilized as a protecting group in peptide synthesis. Its action target involves the protection of the thiol group of L-cysteine during chemical reactions. The mode of action includes adding the trityl (triphenylmethyl) group to the thiol group of L-cysteine, shielding it from unwanted reactions, and enabling specific chemical transformations. Pharmacologically, S-Trityl-L-cysteine itself does not have direct medical applications. Instead, it serves as a valuable tool in organic synthesis, particularly in peptide chemistry, where the trityl protecting group is used to protect and manipulate the reactivity of thiol groups in peptides.