methyl S-methyl-L-cysteinate(SALTDATA: HCl)

Base Information

• Chemical Name: methyl S-methyl-L-cysteinate(SALTDATA: HCl)
• CAS No.: 3830-10-2
• Molecular Formula: C₅H₁₁NO₂S
• Molecular Weight: 149.214
• Mol file: 3830-10-2.mol

Synonyms:methyl S-methyl-L-cysteinate(SALTDATA: HCl)

Chemical Property of methyl S-methyl-L-cysteinate(SALTDATA: HCl)

Chemical Property:

• Boiling Point: 223.1±30.0 °C(Predicted)
• PKA: 6.03±0.33(Predicted)
• PSA: 77.62000
• Density: 1.125±0.06 g/cm3(Predicted)
• LogP: 0.55000

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of methyl S-methyl-L-cysteinate(SALTDATA: HCl)

There total 2 articles about methyl S-methyl-L-cysteinate(SALTDATA: HCl) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

methanol (67-56-1) + S-methyl-L-cysteine (1187-84-4,7728-98-5) → methyl (R)-2-amino-3-methylthiopropanoate (3830-10-2)

Guidance literature:

With thionyl chloride;

DOI:10.1039/jr9640000824

Reference yield:

L-Cysteine (52-90-4) + methyl iodide (74-88-4) → methyl (R)-2-amino-3-methylthiopropanoate (3830-10-2)

Guidance literature:

With sodium hydroxide;

DOI:10.1002/jlac.197419740605

Reference yield:

N-tert-butoxycarbonyl-L-phenylalanine (13734-34-4) + methyl (R)-2-amino-3-methylthiopropanoate (3830-10-2) → C19H28N2O5S (109985-04-8)

Guidance literature:

With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 16h;

DOI:10.1016/j.tet.2010.05.070

upstream raw materials:

methanol

S-methyl-L-cysteine

L-Cysteine

methyl iodide

Downstream raw materials:

C₁₉H₂₈N₂O₅S

Refernces

• 1、 Tiburcio, Estefanía,Greco, Rossella,Mon, Marta,Ballesteros-Soberanas, Jordi,Ferrando-Soria, Jesús,López-Haro, Miguel,Hernández-Garrido, Juan Carlos,Oliver-Meseguer, Judit,Marini, Carlo,Boronat, Mercedes,Armentano, Donatella,Leyva-Pérez, Antonio,Pardo, Emilio. "Soluble/MOF-Supported Palladium Single Atoms Catalyze the Ligand-, Additive-, and Solvent-Free Aerobic Oxidation of Benzyl Alcohols to Benzoic Acids". supporting information. p. 2581 - 2592. Retrieved 2021/02/16.
• 2、 Scully, Conor C.G.,Rutledge, Peter J.. "Synthesis and electrochemical studies of disubstituted ferrocene/dipeptide conjugates with sulfur-containing side chains". scheme or table. p. 5653 - 5659. Retrieved 2010/10/02.