Nialamide

Base Information

• Chemical Name: Nialamide
• CAS No.: 51-12-7
• Molecular Formula: C16H18 N4 O2
• Molecular Weight: 298.345
• Hs Code.: 2933399090
• European Community (EC) Number: 200-079-3
• NSC Number: 759298,124514
• UNII: T2Q0RYM725
• DSSTox Substance ID: DTXSID1023362
• Nikkaji Number: J2.302G
• Wikipedia: Nialamide
• Wikidata: Q2359711
• NCI Thesaurus Code: C80970
• Metabolomics Workbench ID: 149251
• ChEMBL ID: CHEMBL1256841
• Mol file: 51-12-7.mol

Synonyms:Nialamide

Chemical Property of Nialamide

Chemical Property:

• Vapor Pressure: 1.19E-11mmHg at 25°C
• Melting Point: 152-154 °C(lit.)
• Refractive Index: 1.6000 (estimate)
• Boiling Point: 538.1°Cat760mmHg
• PKA: 11.13±0.23(Predicted)
• Flash Point: 279.2°C
• PSA: 83.12000
• Density: 1.203g/cm³
• LogP: 2.19520
• Storage Temp.: −20°C
• Solubility.: ethanol: clear to hazy
• XLogP3: 0.9
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 7
• Exact Mass: 298.14297583
• Heavy Atom Count: 22
• Complexity: 350

Purity/Quality:

98%,99%, ^*data from raw suppliers

Nialamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Toxic in overdose.
• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38-40
• Safety Statements: 22-26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CNC(=O)CCNNC(=O)C2=CC=NC=C2
• Uses: MAO inhibitor Nialamide is a nonselective monoamine oxidase (MAO) inhibitor that is used as an antidepressant.
• Therapeutic Function: Antidepressant

Technology Process of Nialamide

There total 1 articles about Nialamide 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:

→ nialamide (51-12-7)

Guidance literature:

Isonicotinoylhydrazin, N-Benzylacrylamid, Ethylenglykol;