Mimosine

Base Information

• Chemical Name: Mimosine
• CAS No.: 2116-55-4
• Deprecated CAS: 10182-82-8
• Molecular Formula: C₈H₁₀N₂O₄
• Molecular Weight: 198.178
• NSC Number: 159548,69188
• UNII: X9W047UL80
• DSSTox Substance ID: DTXSID80950337
• Nikkaji Number: J51.339C
• Wikipedia: Mimosine
• Wikidata: Q27166999
• ChEMBL ID: CHEMBL251433
• Mol file: 2116-55-4.mol

Synonyms:Leucaenine;Leucaenol;Leucenine;Leucenol;Mimosine

Chemical Property of Mimosine

Chemical Property:

• Boiling Point: 428.6°Cat760mmHg
• Flash Point: 213°C
• PSA: 105.55000
• Density: 1.544g/cm³
• LogP: -0.33390
• XLogP3: -3.5
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 3
• Exact Mass: 198.06405680
• Heavy Atom Count: 14
• Complexity: 321

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CN(C=C(C1=O)O)CC(C(=O)O)N

Technology Process of Mimosine

There total 3 articles about Mimosine 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:

3-methoxy-4(1H)-pyridone (50700-60-2) → mimosine (2116-55-4,10182-82-8)

Guidance literature:

With 1,4-dioxane; Erhitzen des Reaktionsprodukts mit wss.Jodwasserstoffsaeure;

DOI:10.1021/ja01170a092 DOI:10.1139/v62-210

Reference yield:

→ mimosine (2116-55-4,10182-82-8)

Guidance literature:

With water;

DOI:10.1021/ja01170a092

Reference yield:

→ mimosine (2116-55-4,10182-82-8)

Guidance literature:

DL-β-(3-Benzyloxy-4-oxo-1,4-dihydro-1-pyridyl)-α-tosylamino-propionsaeure, Phenol, 1) HBr/AcOH, 2) H2O (Extraktion), 3) Aktivkohle, NH3 bis pH 5 (isoliert als Monohydrat);

DOI:10.1071/CH9761335

upstream raw materials:

3-methoxy-4(1H)-pyridone