N~2~-Acetyl-N-methyl-L-methioninamide

Base Information

Chemical Name:N~2~-Acetyl-N-methyl-L-methioninamide
CAS No.:29744-03-4
Molecular Formula:C₈H₁₆N₂O₂S
Molecular Weight:204.293
Hs Code.:
DSSTox Substance ID:DTXSID00551688
Nikkaji Number:J1.415.422A
Wikidata:Q82431485
Mol file:29744-03-4.mol

Synonyms:29744-03-4;N~2~-Acetyl-N-methyl-L-methioninamide;(2S)-2-acetamido-N-methyl-4-methylsulfanylbutanamide;Butanamide, 2-(acetylamino)-N-methyl-4-(methylthio)-, (2S)-;(S)-2-Acetamido-N-methyl-4-(methylthio)butanamide;(2S)-2-acetamido-N-methyl-4-(methylsulfanyl)butanamide;DTXSID00551688;N-acetyl methionine-N-methyl amide;EN300-344536

Suppliers and Price of N~2~-Acetyl-N-methyl-L-methioninamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
(2S)-2-acetamido-N-methyl-4-(methylsulfanyl)butanamide
100mg
$ 330.00

TRC
(2S)-2-acetamido-N-methyl-4-(methylsulfanyl)butanamide
50mg
$ 220.00

TRC
(2S)-2-acetamido-N-methyl-4-(methylsulfanyl)butanamide
10mg
$ 65.00

Total 3 raw suppliers

Chemical Property of N~2~-Acetyl-N-methyl-L-methioninamide

Chemical Property:

Melting Point:180.9-181.5 °C (sublm)
Boiling Point:490.1±40.0 °C(Predicted)
PSA：90.48000
Density:1.093±0.06 g/cm3(Predicted)
LogP:1.67080
XLogP3:-0.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:204.09324893
Heavy Atom Count:13
Complexity:185

Purity/Quality:

99% ^*data from raw suppliers

(2S)-2-acetamido-N-methyl-4-(methylsulfanyl)butanamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC(CCSC)C(=O)NC
Isomeric SMILES:CC(=O)N[C@@H](CCSC)C(=O)NC

Technology Process of N~2~-Acetyl-N-methyl-L-methioninamide

There total 2 articles about N~2~-Acetyl-N-methyl-L-methioninamide 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: